Aggressive Angiomyxoma in Males
Identifieur interne : 002055 ( Pmc/Curation ); précédent : 002054; suivant : 002056Aggressive Angiomyxoma in Males
Auteurs : Priyadarshini Dehuri ; Debasis Gochhait ; Bh Srinivas ; Sarath Chandra SistlaSource :
- Journal of Clinical and Diagnostic Research : JCDR [ 2249-782X ] ; 2017.
Abstract
Paratesticular aggressive angiomyxoma is a very rare tumour in males. Most of documented cases of aggressive angiomyxomas have been seen in genital, perineal and pelvic regions in women of child bearing age. We report two cases of aggressive angiomyxomas in males who presented with inguinal swellings. A globular mass with greyish white, glistening cut surface was received after excision of the mass. Microscopic examination revealed a paucicellular tumour comprising of spindle shaped cells along with vessels of varying calibre. The accompanying stroma was myxocollagenous. In addition there was evidence of fat infiltration in one of the cases. Immunohistochemical staining showed CD34, desmin, vimetin positivity and negative staining for S100, actin, Estrogen Receptors (ER) and Progesterone Receptors (PR). The microscopic and immunohistochemical features favoured the diagnosis of aggressive angiomyxoma. This report of angiomyxoma in two cases of males assumes great significance in view of the extreme rarity of the tumour in males and its locally infiltrative nature.
Url:
DOI: 10.7860/JCDR/2017/26738.9960
PubMed: 28764175
PubMed Central: 5535368
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Most of documented cases of aggressive angiomyxomas have been seen in genital, perineal and pelvic regions in women of child bearing age. We report two cases of aggressive angiomyxomas in males who presented with inguinal swellings. A globular mass with greyish white, glistening cut surface was received after excision of the mass. Microscopic examination revealed a paucicellular tumour comprising of spindle shaped cells along with vessels of varying calibre. The accompanying stroma was myxocollagenous. In addition there was evidence of fat infiltration in one of the cases. Immunohistochemical staining showed CD34, desmin, vimetin positivity and negative staining for S100, actin, Estrogen Receptors (ER) and Progesterone Receptors (PR). The microscopic and immunohistochemical features favoured the diagnosis of aggressive angiomyxoma. This report of angiomyxoma in two cases of males assumes great significance in view of the extreme rarity of the tumour in males and its locally infiltrative nature.</p></div></front></TEI><pmc article-type="case-report"><pmc-comment>The publisher of this article does not allow downloading of the full text in XML form.</pmc-comment>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Clin Diagn Res</journal-id><journal-id journal-id-type="iso-abbrev">J Clin Diagn Res</journal-id><journal-id journal-id-type="hwp">Journal of Clinical and Diagnostic Research</journal-id><journal-id journal-id-type="publisher-id">JCDR</journal-id><journal-title-group><journal-title>Journal of Clinical and Diagnostic Research : JCDR</journal-title></journal-title-group><issn pub-type="ppub">2249-782X</issn><issn pub-type="epub">0973-709X</issn><publisher><publisher-name>JCDR Research and Publications (P) Limited</publisher-name><publisher-loc>Delhi, India</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">28764175</article-id><article-id pub-id-type="pmc">5535368</article-id><article-id pub-id-type="doi">10.7860/JCDR/2017/26738.9960</article-id><article-categories><subj-group subj-group-type="heading"><subject>Pathology Section</subject><subj-group subj-group-type="heading"><subject>Case Report</subject></subj-group></subj-group></article-categories><title-group><article-title>Aggressive Angiomyxoma in Males</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Dehuri</surname><given-names>Priyadarshini</given-names></name><xref ref-type="aff" rid="aff1">1</xref></contrib><contrib contrib-type="author" corresp="yes"><name><surname>Gochhait</surname><given-names>Debasis</given-names></name><xref ref-type="aff" rid="aff2">2</xref><xref ref-type="corresp" rid="cor1"></xref></contrib><contrib contrib-type="author"><name><surname>Srinivas</surname><given-names>BH</given-names></name><xref ref-type="aff" rid="aff3">3</xref></contrib><contrib contrib-type="author"><name><surname>Sistla</surname><given-names>Sarath Chandra</given-names></name><xref ref-type="aff" rid="aff4">4</xref></contrib></contrib-group><aff id="aff1"><label>1</label> Senior Resident, Department of Pathology,<institution>Jawaharlal Institute of Postgraduate Medical Education and Research</institution>,<addr-line>Puducherry, Pondicherry, India</addr-line>.</aff><aff id="aff2"><label>2</label> Assistant Professor, Department of Pathology,<institution>Jawaharlal Institute of Postgraduate Medical Education and Research</institution>,<addr-line>Puducherry, Pondicherry, India</addr-line>.</aff><aff id="aff3"><label>3</label> Associate Professor, Department of Pathology,<institution>Jawaharlal Institute of Postgraduate Medical Education and Research</institution>,<addr-line>Puducherry, Pondicherry, India</addr-line>.</aff><aff id="aff4"><label>4</label> Professor, Department of Surgery,<institution>Jawaharlal Institute of Postgraduate Medical Education and Research</institution>,<addr-line>Puducherry, Pondicherry, India</addr-line>.</aff><author-notes><corresp id="cor1">NAME, ADDRESS, E-MAIL ID OF THE CORRESPONDING AUTHOR: Dr. Debasis Gochhait, Department of Pathology, Institute Block 2<sup>nd</sup> Floor, JIPMER-605006, Pondicherry, India. E-mail: <email>Debasis.go@gmail.com</email></corresp></author-notes><pub-date pub-type="ppub"><month>6</month><year>2017</year></pub-date><pub-date pub-type="epub"><day>01</day><month>6</month><year>2017</year></pub-date><volume>11</volume><issue>6</issue><fpage>ED01</fpage><lpage>ED03</lpage><history><date date-type="received"><day>12</day><month>1</month><year>2017</year></date><date date-type="rev-request"><day>09</day><month>2</month><year>2017</year></date><date date-type="accepted"><day>06</day><month>3</month><year>2017</year></date></history><permissions><copyright-statement>© 2017 Journal of Clinical and Diagnostic Research</copyright-statement><copyright-year>2017</copyright-year></permissions><abstract><p>Paratesticular aggressive angiomyxoma is a very rare tumour in males. Most of documented cases of aggressive angiomyxomas have been seen in genital, perineal and pelvic regions in women of child bearing age. We report two cases of aggressive angiomyxomas in males who presented with inguinal swellings. A globular mass with greyish white, glistening cut surface was received after excision of the mass. Microscopic examination revealed a paucicellular tumour comprising of spindle shaped cells along with vessels of varying calibre. The accompanying stroma was myxocollagenous. In addition there was evidence of fat infiltration in one of the cases. Immunohistochemical staining showed CD34, desmin, vimetin positivity and negative staining for S100, actin, Estrogen Receptors (ER) and Progesterone Receptors (PR). The microscopic and immunohistochemical features favoured the diagnosis of aggressive angiomyxoma. This report of angiomyxoma in two cases of males assumes great significance in view of the extreme rarity of the tumour in males and its locally infiltrative nature.</p></abstract><kwd-group><kwd>Locally infiltrative</kwd><kwd>Paratesticular</kwd><kwd>Paucicellular</kwd></kwd-group></article-meta></front></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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