Unsuspected chylous ascites in an asymptomatic case of Rosai Dorfman disease.
Identifieur interne : 001C02 ( PubMed/Corpus ); précédent : 001C01; suivant : 001C03Unsuspected chylous ascites in an asymptomatic case of Rosai Dorfman disease.
Auteurs : S. Padma ; P Shanmuga Sundaram ; K Sanjay BabuSource :
- Clinical nuclear medicine [ 1536-0229 ] ; 2013.
English descriptors
- KwdEn :
- MESH :
- complications : Chylous Ascites, Histiocytosis, Sinus.
- diagnostic imaging : Chylous Ascites.
- Asymptomatic Diseases, Female, Humans, Incidental Findings, Lymphoscintigraphy, Middle Aged.
Abstract
Rosai-Dorfman disease, or sinus histiocytosis, first described in 1969, is a benign systemic disorder of histiocytes of unknown etiology characterized by massive lymphadenopathy. It predominantly involves the head and neck region, and is often associated with extranodal involvement. Patient presented to pulmonology with history of sudden onset dyspnea. Clinically and radiologically, the lungs were normal. D-dimer test was noncontributory. As the patient had a family history of lymphedema, lymphoscintigraphy was sought. We report the detection of an unsuspected case of Rosai-Dorfman disease by lower limb lymphoscintigraphy.
DOI: 10.1097/RLU.0b013e3182868230
PubMed: 23567282
Links to Exploration step
pubmed:23567282Le document en format XML
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<author><name sortKey="Padma, S" sort="Padma, S" uniqKey="Padma S" first="S" last="Padma">S. Padma</name>
<affiliation><nlm:affiliation>Department of Nuclear Medicine & PET CT, Amrita Institute of Medical Sciences, Cochin, Kerala, India. padmas@aims.amrita.edu</nlm:affiliation>
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<author><name sortKey="Sundaram, P Shanmuga" sort="Sundaram, P Shanmuga" uniqKey="Sundaram P" first="P Shanmuga" last="Sundaram">P Shanmuga Sundaram</name>
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<author><name sortKey="Babu, K Sanjay" sort="Babu, K Sanjay" uniqKey="Babu K" first="K Sanjay" last="Babu">K Sanjay Babu</name>
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<author><name sortKey="Padma, S" sort="Padma, S" uniqKey="Padma S" first="S" last="Padma">S. Padma</name>
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<author><name sortKey="Sundaram, P Shanmuga" sort="Sundaram, P Shanmuga" uniqKey="Sundaram P" first="P Shanmuga" last="Sundaram">P Shanmuga Sundaram</name>
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<author><name sortKey="Babu, K Sanjay" sort="Babu, K Sanjay" uniqKey="Babu K" first="K Sanjay" last="Babu">K Sanjay Babu</name>
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<series><title level="j">Clinical nuclear medicine</title>
<idno type="eISSN">1536-0229</idno>
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<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Asymptomatic Diseases</term>
<term>Chylous Ascites (complications)</term>
<term>Chylous Ascites (diagnostic imaging)</term>
<term>Female</term>
<term>Histiocytosis, Sinus (complications)</term>
<term>Humans</term>
<term>Incidental Findings</term>
<term>Lymphoscintigraphy</term>
<term>Middle Aged</term>
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<keywords scheme="MESH" qualifier="complications" xml:lang="en"><term>Chylous Ascites</term>
<term>Histiocytosis, Sinus</term>
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<keywords scheme="MESH" qualifier="diagnostic imaging" xml:lang="en"><term>Chylous Ascites</term>
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<keywords scheme="MESH" xml:lang="en"><term>Asymptomatic Diseases</term>
<term>Female</term>
<term>Humans</term>
<term>Incidental Findings</term>
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<front><div type="abstract" xml:lang="en">Rosai-Dorfman disease, or sinus histiocytosis, first described in 1969, is a benign systemic disorder of histiocytes of unknown etiology characterized by massive lymphadenopathy. It predominantly involves the head and neck region, and is often associated with extranodal involvement. Patient presented to pulmonology with history of sudden onset dyspnea. Clinically and radiologically, the lungs were normal. D-dimer test was noncontributory. As the patient had a family history of lymphedema, lymphoscintigraphy was sought. We report the detection of an unsuspected case of Rosai-Dorfman disease by lower limb lymphoscintigraphy.</div>
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<Title>Clinical nuclear medicine</Title>
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<ArticleTitle>Unsuspected chylous ascites in an asymptomatic case of Rosai Dorfman disease.</ArticleTitle>
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<Abstract><AbstractText>Rosai-Dorfman disease, or sinus histiocytosis, first described in 1969, is a benign systemic disorder of histiocytes of unknown etiology characterized by massive lymphadenopathy. It predominantly involves the head and neck region, and is often associated with extranodal involvement. Patient presented to pulmonology with history of sudden onset dyspnea. Clinically and radiologically, the lungs were normal. D-dimer test was noncontributory. As the patient had a family history of lymphedema, lymphoscintigraphy was sought. We report the detection of an unsuspected case of Rosai-Dorfman disease by lower limb lymphoscintigraphy.</AbstractText>
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