Type D lymphomatoid papulosis simulating aggressive epidermotropic cytotoxic lymphoma.

dc.contributor.authorMani, Venkatraman
dc.contributor.authorGeorge, Renu
dc.contributor.authorVijayakumar, Kavita
dc.contributor.authorNair, Sheila
dc.date.accessioned2016-08-11T11:34:16Z
dc.date.available2016-08-11T11:34:16Z
dc.date.issued2016-01
dc.description.abstractThree histological subtypes of lymphomatoid papulosis (LyP), type A (histiocytic), type B (mycosis fungoides like) and type C (anaplastic large cell lymphoma like) are well recognized. Two new histological variants, type D (simulating an aggressive epidermotropic cytotoxic lymphoma) and type E (angioinvasive type) has been described recently. We describe a 27‑year‑old man presented with a history of asymptomatic erythematous papules on both upper and lower limbs noted since 10 years of age. There were no systemic symptoms. Biopsy revealed an atypical dermal lymphoid infiltrate with epidermotropism, and the immunohistochemical markers showed a diffuse positivity for CD3, CD8, CD56, T1A and granzyme B with the focal positivity of CD30. All other relevant tests were normal. In this case report of a recently described delineated variant of LyP we emphasize the indolent course of this entity although the histology would suggest a more aggressive disease.en_US
dc.identifier.citationMani Venkatraman, George Renu, Vijayakumar Kavita, Nair Sheila. Type D lymphomatoid papulosis simulating aggressive epidermotropic cytotoxic lymphoma. Indian Journal of Pathology & Microbiology. 2016 Jan-Mar 59(1): 81-83.en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/176638
dc.language.isoenen_US
dc.source.urihttps://www.ijpmonline.org/article.asp?issn=0377-4929;year=2016;volume=59;issue=1;spage=81;epage=83;aulast=Manien_US
dc.subjectCD30 lymphomasen_US
dc.subjectcutaneous lymphomaen_US
dc.subjectlymphomatoid papulosisen_US
dc.titleType D lymphomatoid papulosis simulating aggressive epidermotropic cytotoxic lymphoma.en_US
dc.typeArticleen_US
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