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Effect of antiretroviral therapy on mucocutaneous manifestations among Human Immunodeficiency Virus-infected patients in a tertiary care centre in South India

Identifieur interne : 000098 ( Pmc/Corpus ); précédent : 000097; suivant : 000099

Effect of antiretroviral therapy on mucocutaneous manifestations among Human Immunodeficiency Virus-infected patients in a tertiary care centre in South India

Auteurs : Nagendran Prabhakaran ; Telanseri J. Jaisankar ; Abdoul Hamide ; Munisamy Malathi ; Rashmi Kumari ; Devinder Mohan Thappa

Source :

RBID : PMC:4660558

Abstract

Background:

Human Immunodeficiency Virus (HIV) infection produces a wide range of infectious and noninfectious dermatoses which correlate with the degree of immunodeficiency. Since the introduction of highly active antiretroviral therapy (HAART), there has been a dramatic decrease in the incidence of HIV-associated dermatoses. However, HAART itself causes various cutaneous adverse drug reactions.

Aims:

To assess the various mucocutaneous manifestations in HIV-infected individuals and its association with CD4 count and to assess the effect of HAART on mucocutaneous manifestations.

Materials and Methods:

Of the 170 patients recruited, 110 patients were previously diagnosed with HIV and were on follow-up. The rest 60 patients were newly diagnosed cases at recruitment, and these patients were followed up every month for mucocutaneous manifestations for a period of 6 months.

Results:

Of the 170 patients screened, 69.41% patients had at least one mucocutaneous lesion at presentation. Fungal, viral, and bacterial infections were observed present in 17.6%, 10.6%, and 9.4% patients, respectively. There was a significant difference in the occurrence of candidal infections in the HAART versus non-HAART group (P = 0.0002). Candidiasis (P ≤ 0.0001) and human papillomavirus infection (P = 0.0475) occurred more commonly with CD4 count <200 cells/mm 3 . Among the noninfectious dermatoses, inflammatory dermatoses (17.6%) were more commonly observed at recruitment followed by adverse cutaneous drug reactions (16.5%) and neoplasms (5.3%).

Conclusion:

HAART has significantly altered the patterns of mucocutaneous manifestations. The prevalence of both infectious and inflammatory dermatoses has come down. However, there is an increase in the incidence of adverse cutaneous drug reactions.


Url:
DOI: 10.4103/0253-7184.167160
PubMed: 26692610
PubMed Central: 4660558

Links to Exploration step

PMC:4660558

Le document en format XML

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<name sortKey="Prabhakaran, Nagendran" sort="Prabhakaran, Nagendran" uniqKey="Prabhakaran N" first="Nagendran" last="Prabhakaran">Nagendran Prabhakaran</name>
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<name sortKey="Hamide, Abdoul" sort="Hamide, Abdoul" uniqKey="Hamide A" first="Abdoul" last="Hamide">Abdoul Hamide</name>
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<name sortKey="Malathi, Munisamy" sort="Malathi, Munisamy" uniqKey="Malathi M" first="Munisamy" last="Malathi">Munisamy Malathi</name>
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<nlm:aff id="aff1">Department of Dermatology, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry, India</nlm:aff>
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<name sortKey="Kumari, Rashmi" sort="Kumari, Rashmi" uniqKey="Kumari R" first="Rashmi" last="Kumari">Rashmi Kumari</name>
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<nlm:aff id="aff1">Department of Dermatology, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry, India</nlm:aff>
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<name sortKey="Thappa, Devinder Mohan" sort="Thappa, Devinder Mohan" uniqKey="Thappa D" first="Devinder Mohan" last="Thappa">Devinder Mohan Thappa</name>
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<title>Background:</title>
<p>Human Immunodeficiency Virus (HIV) infection produces a wide range of infectious and noninfectious dermatoses which correlate with the degree of immunodeficiency. Since the introduction of highly active antiretroviral therapy (HAART), there has been a dramatic decrease in the incidence of HIV-associated dermatoses. However, HAART itself causes various cutaneous adverse drug reactions.</p>
</sec>
<sec id="st2">
<title>Aims:</title>
<p>To assess the various mucocutaneous manifestations in HIV-infected individuals and its association with CD4 count and to assess the effect of HAART on mucocutaneous manifestations.</p>
</sec>
<sec id="st3">
<title>Materials and Methods:</title>
<p>Of the 170 patients recruited, 110 patients were previously diagnosed with HIV and were on follow-up. The rest 60 patients were newly diagnosed cases at recruitment, and these patients were followed up every month for mucocutaneous manifestations for a period of 6 months.</p>
</sec>
<sec id="st4">
<title>Results:</title>
<p>Of the 170 patients screened, 69.41% patients had at least one mucocutaneous lesion at presentation. Fungal, viral, and bacterial infections were observed present in 17.6%, 10.6%, and 9.4% patients, respectively. There was a significant difference in the occurrence of candidal infections in the HAART versus non-HAART group (
<italic>P</italic>
= 0.0002). Candidiasis (
<italic>P</italic>
≤ 0.0001) and human papillomavirus infection (
<italic>P</italic>
= 0.0475) occurred more commonly with CD4 count <200 cells/mm
<sup>3</sup>
. Among the noninfectious dermatoses, inflammatory dermatoses (17.6%) were more commonly observed at recruitment followed by adverse cutaneous drug reactions (16.5%) and neoplasms (5.3%).</p>
</sec>
<sec id="st5">
<title>Conclusion:</title>
<p>HAART has significantly altered the patterns of mucocutaneous manifestations. The prevalence of both infectious and inflammatory dermatoses has come down. However, there is an increase in the incidence of adverse cutaneous drug reactions.</p>
</sec>
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<pmc article-type="research-article">
<pmc-dir>properties open_access</pmc-dir>
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Indian J Sex Transm Dis</journal-id>
<journal-id journal-id-type="iso-abbrev">Indian J Sex Transm Dis</journal-id>
<journal-id journal-id-type="publisher-id">IJSTD</journal-id>
<journal-title-group>
<journal-title>Indian Journal of Sexually Transmitted Diseases</journal-title>
</journal-title-group>
<issn pub-type="ppub">0253-7184</issn>
<issn pub-type="epub">1998-3816</issn>
<publisher>
<publisher-name>Medknow Publications & Media Pvt Ltd</publisher-name>
<publisher-loc>India</publisher-loc>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="pmid">26692610</article-id>
<article-id pub-id-type="pmc">4660558</article-id>
<article-id pub-id-type="publisher-id">IJSTD-36-166</article-id>
<article-id pub-id-type="doi">10.4103/0253-7184.167160</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Original Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Effect of antiretroviral therapy on mucocutaneous manifestations among Human Immunodeficiency Virus-infected patients in a tertiary care centre in South India</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname>Prabhakaran</surname>
<given-names>Nagendran</given-names>
</name>
<xref ref-type="aff" rid="aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Jaisankar</surname>
<given-names>Telanseri J.</given-names>
</name>
<xref ref-type="aff" rid="aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Hamide</surname>
<given-names>Abdoul</given-names>
</name>
<xref ref-type="aff" rid="aff2">1</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Malathi</surname>
<given-names>Munisamy</given-names>
</name>
<xref ref-type="aff" rid="aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Kumari</surname>
<given-names>Rashmi</given-names>
</name>
<xref ref-type="aff" rid="aff1"></xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Thappa</surname>
<given-names>Devinder Mohan</given-names>
</name>
<xref ref-type="aff" rid="aff1"></xref>
<xref ref-type="corresp" rid="cor1"></xref>
</contrib>
</contrib-group>
<aff id="aff1">Department of Dermatology, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry, India</aff>
<aff id="aff2">
<label>1</label>
Department of Medicine, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry, India</aff>
<author-notes>
<corresp id="cor1">
<bold>Address for correspondence:</bold>
Dr. Devinder Mohan Thappa, Department of Dermatology, Jawaharlal Institute of Post Graduate Medical Education and Research, Puducherry, India. E-mail:
<email xlink:href="dmthappa@gmail.com">dmthappa@gmail.com</email>
</corresp>
</author-notes>
<pub-date pub-type="ppub">
<season>Jul-Dec</season>
<year>2015</year>
</pub-date>
<volume>36</volume>
<issue>2</issue>
<fpage>166</fpage>
<lpage>173</lpage>
<permissions>
<copyright-statement>Copyright: © Indian Journal of Sexually Transmitted Diseases and AIDS</copyright-statement>
<copyright-year>2015</copyright-year>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by-nc-sa/3.0">
<license-p>This is an open access article distributed under the terms of the Creative Commons Attribution NonCommercial ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non commercially, as long as the author is credited and the new creations are licensed under the identical terms.</license-p>
</license>
</permissions>
<abstract>
<sec id="st1">
<title>Background:</title>
<p>Human Immunodeficiency Virus (HIV) infection produces a wide range of infectious and noninfectious dermatoses which correlate with the degree of immunodeficiency. Since the introduction of highly active antiretroviral therapy (HAART), there has been a dramatic decrease in the incidence of HIV-associated dermatoses. However, HAART itself causes various cutaneous adverse drug reactions.</p>
</sec>
<sec id="st2">
<title>Aims:</title>
<p>To assess the various mucocutaneous manifestations in HIV-infected individuals and its association with CD4 count and to assess the effect of HAART on mucocutaneous manifestations.</p>
</sec>
<sec id="st3">
<title>Materials and Methods:</title>
<p>Of the 170 patients recruited, 110 patients were previously diagnosed with HIV and were on follow-up. The rest 60 patients were newly diagnosed cases at recruitment, and these patients were followed up every month for mucocutaneous manifestations for a period of 6 months.</p>
</sec>
<sec id="st4">
<title>Results:</title>
<p>Of the 170 patients screened, 69.41% patients had at least one mucocutaneous lesion at presentation. Fungal, viral, and bacterial infections were observed present in 17.6%, 10.6%, and 9.4% patients, respectively. There was a significant difference in the occurrence of candidal infections in the HAART versus non-HAART group (
<italic>P</italic>
= 0.0002). Candidiasis (
<italic>P</italic>
≤ 0.0001) and human papillomavirus infection (
<italic>P</italic>
= 0.0475) occurred more commonly with CD4 count <200 cells/mm
<sup>3</sup>
. Among the noninfectious dermatoses, inflammatory dermatoses (17.6%) were more commonly observed at recruitment followed by adverse cutaneous drug reactions (16.5%) and neoplasms (5.3%).</p>
</sec>
<sec id="st5">
<title>Conclusion:</title>
<p>HAART has significantly altered the patterns of mucocutaneous manifestations. The prevalence of both infectious and inflammatory dermatoses has come down. However, there is an increase in the incidence of adverse cutaneous drug reactions.</p>
</sec>
</abstract>
<kwd-group>
<kwd>Antiretroviral therapy</kwd>
<kwd>CD4 count</kwd>
<kwd>Human Immunodeficiency Virus infection</kwd>
<kwd>mucocutaneous manifestations</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec1-1">
<title>INTRODUCTION</title>
<p>Human Immunodeficiency Virus (HIV) is nearly 33 years old and dermatological manifestations occur throughout the course of HIV infection ranging from the maculopapular rash seen with acute primary HIV infection/seroconversion to the disseminated mycoses and malignancies seen with advanced disease. These mucocutaneous lesions usually correlate with the degree of immunodeficiency.</p>
<p>Following the introduction of highly active antiretroviral therapy (HAART) since 1996, there has been a dramatic decrease in the incidence and severity of HIV-associated dermatoses. The pervasive use of HAART may also have changed the patterns and rates of HIV-related cutaneous manifestations.[
<xref rid="ref1" ref-type="bibr">1</xref>
] Although, mucocutaneous lesions have diminished in their frequency following the introduction of HAART, the therapy itself can lead to increased incidence of adverse cutaneous drug reactions.[
<xref rid="ref2" ref-type="bibr">2</xref>
] Hence, we undertook this study to study the various mucocutaneous manifestations encountered in treatment-naïve HIV-infected individuals and those on HAART.</p>
</sec>
<sec sec-type="materials|methods" id="sec1-2">
<title>MATERIALS AND METHODS</title>
<p>This was a hospital-based descriptive study done in HIV-infected patients attending antiretroviral therapy (ART) clinic, Suraksha clinic (Sexually Transmitted Diseases Clinic) and Dermatology Outpatient Department, JIPMER, Puducherry from November 2012 to May 2014, after obtaining Institute Ethics Committee clearance (IEC/SC/2012/4/113).</p>
<p>One hundred and seventy HIV seropositive patients irrespective of gender, age were included in the study. Among them, 110 patients were previously diagnosed with HIV and were on follow-up for 6 months. Of these, 100 patients were already initiated on HAART (mean duration of HAART 4.9 years ranging from 4 months to 25 years) and the rest 10 were not on HAART. The rest 60 patients were newly diagnosed cases at recruitment, and these patients were followed up every month for mucocutaneous manifestations for a period of 6 months. Of these 60 patients, 48 patients received HAART [
<xref ref-type="fig" rid="D1">Flow Diagram 1</xref>
].</p>
<fig id="D1" position="float">
<label>Flow Diagram 1</label>
<caption>
<p>Status of the Human Immunodeficiency Virus seropositive cases at the time of recruitment and follow-up</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g001"></graphic>
</fig>
<p>The diagnosis was made based on history, clinical examination, and laboratory investigations (KOH, Tzanck, and biopsy) wherever necessary. The CD4 count was done for all the patients at recruitment and after 6 months.</p>
<sec id="sec2-1">
<title>Statistical analysis</title>
<p>The data collected were tabulated in Microsoft Excel Worksheet, and computer-based analysis was performed using the IBM SPSS (software package for statistical analysis) 20 software (USA). The categorical variables were summarized as proportions and percentages. The continuous variables were summarized as a mean and standard deviation. For comparison of means, unpaired t-test was used for two groups. For comparison of proportions, Fisher's exact test, one-way ANOVA, and McNemar's test were used.</p>
</sec>
</sec>
<sec sec-type="results" id="sec1-3">
<title>RESULTS</title>
<p>The mean age of the study population was 39.88 ± 9.44 years (ranging from 11 to 65 years with a median of 38 years). There was no gender predilection and the male to female ratio was 1.04:1. The demographic characteristics of the 170 HIV-positive patients are depicted in
<xref ref-type="table" rid="T1">Table 1</xref>
. Pulmonary tuberculosis was the most common form of tuberculosis (29 patients, 17.1%). Extrapulmonary tuberculosis was seen in 22 patients (13%).</p>
<table-wrap id="T1" position="float">
<label>Table 1</label>
<caption>
<p>Demographic characteristics of the 170 HIV-positive patients in our study</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g002"></graphic>
</table-wrap>
<sec id="sec2-2">
<title>WHO clinical staging</title>
<p>Most (78 patients; 45.9%) of our patients were in WHO clinical stage 3 during the initial diagnosis. Forty-two patients (24.7%) each was in stage 1 and 4.</p>
</sec>
<sec id="sec2-3">
<title>Highly active antiretroviral therapy regimen</title>
<p>The first line ART, zidovudine (AZT) + lamivudine (3TC) + nevirapine (NEV) was initiated in 101 patients (69.2%). Twenty-four patients (16.4%) were started on AZT + 3TC + efavirenz (EFV) due to co-infection with tuberculosis. Twenty patients were started on stavudine based regimen due to anemia. Other 3 patients were on tenofovir + 3TC + EFV.</p>
</sec>
<sec id="sec2-4">
<title>Mucocutaneous manifestations of the Human Immunodeficiency Virus infected cases</title>
<p>Of the 170 HIV-infected patients screened, 118 (69.41%) patients had at least one mucocutaneous lesion at presentation. Among the infectious dermatoses, fungal infections were the most commonly observed infections present in 30 (17.6%) patients. Viral infections were observed in 18 (10.6%) patients [
<xref ref-type="fig" rid="F1">Figure 1</xref>
] and bacterial infections in 16 (9.4%) patients [
<xref ref-type="fig" rid="F2">Figure 2</xref>
]. A mean number of dermatoses was 1.2/patient. On follow-up of these 170 patients, the mean number of dermatoses increased to 1.75/patient during the entire study period.</p>
<fig id="F1" position="float">
<label>Figure 1</label>
<caption>
<p>Chronic herpes simplex presenting as multiple vesicular and ulcerative lesions in perianal area</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g003"></graphic>
</fig>
<fig id="F2" position="float">
<label>Figure 2</label>
<caption>
<p>Secondary syphilis - multiple nodulo-ulcerative lesions distributed in trunk and extremities</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g004"></graphic>
</fig>
</sec>
<sec id="sec2-5">
<title>Infectious dermatoses</title>
<p>The various infectious dermatoses observed in patients on HAART and not on HAART are provided in
<xref ref-type="table" rid="T2">Table 2</xref>
. Most of the infections had a higher prevalence in patients who did not receive HAART. However, this was significant in the case of fungal infections (11% vs. 27.1%, P: 0.0081).</p>
<table-wrap id="T2" position="float">
<label>Table 2</label>
<caption>
<p>Infectious dermatoses of patients who were on HAART (100 cases) and not on HAART (70 cases) at presentation</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g005"></graphic>
</table-wrap>
<p>The most common infection observed in our study was oral candidiasis, the pseudomembranous type being the most frequently observed. There was a significant difference in the occurrence of candidal infections in the HAART versus non-HAART group (
<italic>P</italic>
= 0.0002) but there was no significant difference in any of the viral or bacterial infections. Viral infections were more common in the HAART group.</p>
</sec>
<sec id="sec2-6">
<title>Infectious dermatoses and mean CD4 correlation</title>
<p>The CD4 count was significantly lower in those who had candidiasis and verruca vulgaris compared to those without these infections. The comparison of mean CD4 count of patients with and without infectious dermatoses is presented in
<xref ref-type="table" rid="T3">Table 3</xref>
.</p>
<table-wrap id="T3" position="float">
<label>Table 3</label>
<caption>
<p>Comparison of mean CD4 count of patients who were having and not having infectious dermatoses</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g006"></graphic>
</table-wrap>
</sec>
<sec id="sec2-7">
<title>Noninfectious dermatoses</title>
<p>Among the noninfectious dermatoses, inflammatory dermatoses (30 patients, 17.6%) were more commonly observed at recruitment followed by adverse cutaneous drug reactions (28 patients, 16.5%) and neoplasms (9 patients, 5.3%). The comparison of noninfectious dermatoses of patients who were on HAART and not on HAART is depicted in
<xref ref-type="table" rid="T4">Table 4</xref>
.</p>
<table-wrap id="T4" position="float">
<label>Table 4</label>
<caption>
<p>Noninfectious dermatoses of patients who were on HAART (100 cases) and not on HAART (70 cases) at presentation</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g007"></graphic>
</table-wrap>
<p>At recruitment 28/170 (16.5%) patients had at least one adverse cutaneous drug reaction. The most common adverse effect noted was AZT induced longitudinal melanonychia [
<xref ref-type="fig" rid="F3">Figure 3</xref>
] and nail pigmentation (9 patients, 5.3%). Seven patients (4.1%) had stavudine induced lipoatrophy, and they were shifted to AZT based regimen. Two patients with NEV induced maculopapular rash and 1 patient with the drug hypersensitivity syndrome were then shifted to EFV based regimen. AZT induced oral lichenoid drug eruption (OLDR) [
<xref ref-type="fig" rid="F4">Figure 4</xref>
] was observed in 4 patients (2.3%). A case of photosensitive lichenoid eruption was seen in a patient who was on AZT for 3 years.</p>
<fig id="F3" position="float">
<label>Figure 3</label>
<caption>
<p>(a) Zidovudine induced pigmentation affecting palms. (b) Zidovudine induced longitudinal melanonychia</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g008"></graphic>
</fig>
<fig id="F4" position="float">
<label>Figure 4</label>
<caption>
<p>(a) Zidovudine induced lichenoid eruption affecting buccal mucosa. (b) Resolution of oral lichenoid eruption after changing zidovudine to tenofovir</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g009"></graphic>
</fig>
</sec>
<sec id="sec2-8">
<title>Noninfectious dermatoses and mean CD4 count correlation</title>
<p>Pruritic papular eruption (PPE) was significantly associated with lower mean CD4 count (194.64 ± 122.04 cells/mm
<sup>3</sup>
) compared with those who were not having PPE (
<italic>P</italic>
= 0.001). OLDR was significantly more in patients with higher CD4 count (626.00 ± 129.75 cells/mm
<sup>3</sup>
). The CD4 count correlation of noninfectious dermatoses is tabulated in
<xref ref-type="table" rid="T5">Table 5</xref>
.</p>
<table-wrap id="T5" position="float">
<label>Table 5</label>
<caption>
<p>Comparison of mean CD4 count of patients who were having versus those not having noninfectious dermatoses</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g010"></graphic>
</table-wrap>
</sec>
<sec id="sec2-9">
<title>Clinical manifestations and CD4 correlation of patients who were newly diagnosed at recruitment</title>
<p>Of the 60 newly diagnosed patients, 48 patients were started on ART and followedup for 6 months. The results are tabulated in
<xref ref-type="table" rid="T6">Table 6</xref>
.</p>
<table-wrap id="T6" position="float">
<label>Table 6</label>
<caption>
<p>Mucocutaneous manifestations and CD4 count of 48 HIV-infected new patients</p>
</caption>
<graphic xlink:href="IJSTD-36-166-g011"></graphic>
</table-wrap>
<p>Before starting HAART, infections were more common (24 patients, 50%). Among them, candidiasis was the most common infection seen in 14 patients (29.2%). Among the inflammatory dermatoses, PPE was more common (6 patients; 12.5%). After starting HAART, the prevalence of infections and inflammatory dermatoses had come down with a significant reduction in fungal infections (
<italic>P</italic>
= 0.007).</p>
<p>The baseline CD4 count of 30/48 patients (62.5%) was <200 cells/mm
<sup>3</sup>
while 15 patients had a CD4 count in the range of 200-350 cells/mm
<sup>3</sup>
. After initiation of HAART, at the end of 6 months only 8 patients had CD4 count <200 and 21 patients had CD4 count more than 200 cells/mm
<sup>3</sup>
.</p>
<p>Among the 12 patients whom ART was not initiated during the study period, 2 patients died due to malignancy at the time of diagnosis. Two patients were lost to follow-up. Rest 8 patients had baseline CD4 count more than 400 cells/mm
<sup>3</sup>
. Among them, 2 patients had condyloma acuminata at the time of diagnosis. During follow-up, none of them developed any new infections.</p>
</sec>
<sec id="sec2-10">
<title>Mortality</title>
<p>Three patients died during the follow-up. Two out of three patients had non-Hodgkin's lymphoma (NHL) in which 1 patient was on HAART. The third one had Kaposi's sarcoma (KS) in an Indian patient, and he was not on HAART.</p>
</sec>
</sec>
<sec sec-type="discussion" id="sec1-4">
<title>DISCUSSION</title>
<p>Dermatological manifestations are not only common but are often a presenting feature of HIV infection, often correlating with the degree of immunodeficiency. The increasing severity and atypical presentation of these dermatological conditions characterize HIV co-infection. After the introduction of HAART therapy, there is a significant decrease in the prevalence of infectious dermatoses and AIDS-defining illnesses (like esophageal candidiasis, chronic herpes simplex [HS], and deep fungal infections). However, there is a parallel increase in the mucocutaneous adverse effects due to drugs in the post-HAART era. Thus, HAART has significantly altered the pattern of mucocutaneous manifestations occurring in HIV patients.</p>
<p>The demographic characteristics of our study showed no gender predilection whereas previous studies showed a male predominance.[
<xref rid="ref3" ref-type="bibr">3</xref>
] This may be attributed to increasing health seeking behavior among the female population. Mean dermatoses in our study population at recruitment were 1.2/patient. In our study, we followed up the patient for 6 months and found mean dermatoses increased to 1.75/patient. This reiterates the fact that drug eruptions showed an increasing trend in the post-HAART era.</p>
<p>Infectious dermatoses are the most common skin manifestations in HIV. In the present study, however only 32.9% patients had infectious dermatoses while 39.1% had noninfectious dermatoses. Though fungal infections were the most common infections occurring in 30 patients (17.6%) followed by viral (10.6%) and bacterial (9.4%) infections in our study, the overall prevalence is low compared to previous studies in the literature.[
<xref rid="ref1" ref-type="bibr">1</xref>
<xref rid="ref2" ref-type="bibr">2</xref>
] This could be attributed to the fact that most of our patients were on HAART.</p>
<p>Oral candidiasis (pseudomembranous type) is the most common mucocutaneous manifestations observed in various studies prior to the administration of HAART which was also the case in our study. The mean CD4 count of patients with candidiasis (120 cells/mm
<sup>3</sup>
) was significantly low compared to those without candidiasis as observed in previous studies wherein candidiasis occurred with low CD4 count (<200 cells/mm
<sup>3</sup>
).[
<xref rid="ref1" ref-type="bibr">1</xref>
<xref rid="ref4" ref-type="bibr">4</xref>
]</p>
<p>The most common viral infection noted was human papillomavirus infection, seen in 10 (5.9%) patients. The mean CD4 count of patients with verruca vulgaris was significantly low compared to those without verruca. Among the sexually transmitted infections, anogential warts were the most common manifestation in a study done by Chopra and Arora[
<xref rid="ref5" ref-type="bibr">5</xref>
] similar to our study wherein we observed 2.4% patients having condyloma acuminata. Condyloma acuminata occurred with a mean CD4 count of 320 cells/mm
<sup>3</sup>
in the study population. There are conflicting reports in the literature regarding correlation of CD4 count and condyloma acuminata. While Kim
<italic>et al</italic>
[
<xref rid="ref6" ref-type="bibr">6</xref>
] found that condyloma acuminata was more prevalent in the patients with a CD4 count >200cells/mm
<sup>3</sup>
, Goldstein
<italic>et al</italic>
[
<xref rid="ref7" ref-type="bibr">7</xref>
] observed condyloma acuminata with advanced immunosuppression (CD4 < 75 cells/mm
<sup>3</sup>
). Hence, it can be inferred that condyloma acuminata can occur in patients with normal CD4 count.</p>
<p>HS and herpes zoster (HZ) occur due to reactivation of latent infection during immunodeficiency. HZ is usually unidermatomal in HIV.[
<xref rid="ref8" ref-type="bibr">8</xref>
] But multidermatomal, disseminated and atypical presentations like necrotic, hemorrhagic and hyperkeratotic lesions do occur in HIV. Though we observed cases of HZ occurring in multidermatomal pattern and as immune reconstitution inflammatory syndrome (IRIS) manifestations, the prevalence was much lower than that reported by previous study[
<xref rid="ref2" ref-type="bibr">2</xref>
] since, most of our patients were on HAART. These findings support the role of HAART in increasing the immunity in HIV-infected patients. HS and molluscum contagiosum (MC) usually occur with lower CD4 count (<200 cells/mm
<sup>3</sup>
).[
<xref rid="ref9" ref-type="bibr">9</xref>
] Although, MC occurred with lower mean CD4 count (75.33 ± 63.53 cells/mm
<sup>3</sup>
) in our study, we found HS to be occurring in those with a higher mean CD4 count (405.00 ± 391.67 cells/mm
<sup>3</sup>
) in contrast to other studies.[
<xref rid="ref1" ref-type="bibr">1</xref>
<xref rid="ref9" ref-type="bibr">9</xref>
]</p>
<p>
<italic>Staphylococcus aureus</italic>
was the most common pathogen implicated in cutaneous and systemic bacterial infection in HIV-infected patients[
<xref rid="ref5" ref-type="bibr">5</xref>
<xref rid="ref8" ref-type="bibr">8</xref>
] which was also observed in our study.</p>
<p>The prevalence of noninfectious dermatoses in our study was 39.1% which is similar to a study done in China.[
<xref rid="ref2" ref-type="bibr">2</xref>
] The spectrum of inflammatory dermatoses seen in HIV varies from PPE, seborrheic dermatitis (SD), and ichthyosis, psoriasis to reactive arthritis. PPE presents as pruritic papules in the face and exposed sites of extremities. Although the pathogenesis is poorly understood, it is said to occur as a hypersensitive response to insect bites. In our study, PPE was the most common inflammatory dermatoses observed and was significantly associated with lower mean CD4 count (194.64 ± 122.04 cells/mm
<sup>3</sup>
) similar to a previous study.[
<xref rid="ref1" ref-type="bibr">1</xref>
] The increased prevalence may be due to poor socioeconomic conditions in our region in which patients are prone to arthropod bites.</p>
<p>SD presents with increased severity varying with the stage of immunodeficiency.[
<xref rid="ref8" ref-type="bibr">8</xref>
] It is one of the most common noninfective dermatoses of HIV, as observed by Jensen
<italic>et al</italic>
[
<xref rid="ref10" ref-type="bibr">10</xref>
] who reported SD in 49.2% patients. However, in our study, only 1.8% (3 patients) had SD probably because most of our patients were on HAART at recruitment. It occurred with a mean CD4 count of 76.33 cells/mm
<sup>3</sup>
in 3 patients.</p>
<p>One of the causes of acquired ichthyosis is AIDS. The prevalence of acquired ichthyosis and xerosis in other studies range from 5% to 10%[
<xref rid="ref3" ref-type="bibr">3</xref>
],
<sup>
<xref rid="ref9" ref-type="bibr">9</xref>
],[</sup>
and initiation of ART reduces the symptoms of ichthyosis.[
<xref rid="ref11" ref-type="bibr">11</xref>
] In our study, population where most of them were on HAART, ichthyosis/xerosis was found in only 3.5% patients and among them only 1 patient had generalized ichthyosis.</p>
<p>AIDS-associated KS presents as widespread cutaneous lesions which may disseminate to involve internal organs and is the most frequent tumor in sub-Saharan African countries.[
<xref rid="ref12" ref-type="bibr">12</xref>
<xref rid="ref13" ref-type="bibr">13</xref>
] In a study done on cutaneous manifestations of HIV 15 years back in our institute no cases of KS was observed.[
<xref rid="ref14" ref-type="bibr">14</xref>
] Similarly, there are only sparse case reports of KS from India. However in the current study, we observed 2 patients with KS. Both cases had disseminated KS. NHL and squamous cell carcinoma were observed in 4 patients each. In the present study, various presentations of NHL observed were chronic ulceration in the axilla with lymphedema, parapharyngeal mass, nodulo-ulcerative lesions, and generalized lymphadenopathy. We had two cases of invasive squamous cell carcinoma cervix. Hence, regular screening for HIV-infected women for cervical malignancies by Pap smear should be emphasized.</p>
<p>Drug rashes such as a maculopapular rash, erythema multiforme, drug hypersensitivity syndrome, Stevens-Johnson syndrome, toxic epidermal necrolysis, and hyperpigmentation are common in HIV patients.[
<xref rid="ref15" ref-type="bibr">15</xref>
] Reactivation of Epstein-Barr virus and cytomegalovirus, glutathione depletion, immune dysregulation like an increase in IgE secreting B cells and increased usage of drugs (polypharmacy) may predispose to increased incidence of a drug reaction in HIV. Adverse cutaneous drug reactions are not only more common but also severe in HIV-infected individuals.[
<xref rid="ref16" ref-type="bibr">16</xref>
] They are the most common side effects seen in patients who were started on HAART (especially NNRTI) within 8.3 months in a study done by Huang
<italic>et al</italic>
[
<xref rid="ref2" ref-type="bibr">2</xref>
]</p>
<p>In our study, adverse reaction to drugs was observed in 28 patients (16.5%). We found longitudinal melanonychia and nail pigmentation (5.2%) as the most common nail change in patients who were on AZT. Stavudine induced lipoatrophy was found in only 4.1% patients whereas Sharma
<italic>et al</italic>
[
<xref rid="ref17" ref-type="bibr">17</xref>
] observed it in 14.5% patients. This was probably due to the predominant initial regimen in our study being AZT based (85.6%).</p>
<p>In the study done by Sreenivasan and Dasegowda[
<xref rid="ref18" ref-type="bibr">18</xref>
] 14% of cases required modification of first-line regimen with NEV induced skin rash being the most common reason. In our study, 3% of patients required regimen change due to NEV induced rash. OLDR was seen in four patients with higher CD4 count (626.00 ± 129.75 cell/mm
<sup>3</sup>
), and there was statistically significant difference in mean CD4 count (
<italic>P</italic>
= 0.007). Previously, Arirachakaran
<italic>et al</italic>
[
<xref rid="ref19" ref-type="bibr">19</xref>
] had reported a case of oral lichenoid eruption that has resolved after stopping AZT. In our study also, we observed the resolution of persistent OLDR on shifting a patient from AZT to tenofovir based regimen.</p>
<p>IRIS is characterized by paradoxical worsening of existing clinical condition or appearance of a new disease following HAART. In the current study, 2 patients had developed IRIS presenting as HZ. Though HIV viral load was not done, both the patients had a significant increase in CD4 count from baseline.</p>
</sec>
<sec sec-type="conclusions" id="sec1-5">
<title>CONCLUSION</title>
<p>Mucocutaneous manifestations are common problems encountered in the HIV-infected patients where infectious dermatoses predominated in the pre-HAART era. After the introduction of HAART, there is a significant alteration in the patterns of mucocutaneous manifestations. The prevalence of both infectious and inflammatory dermatoses has come down. But there is an increase in the incidence of adverse cutaneous drug reactions.</p>
<sec id="sec2-11">
<title>Financial support and sponsorship</title>
<p>Nil.</p>
</sec>
<sec id="sec2-12">
<title>Conflicts of interest</title>
<p>There are no conflicts of interest.</p>
</sec>
</sec>
</body>
<back>
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