Angioplasmocellular hyperplasia is a rare clinical condition with blood vessel proliferation and a reactive plasma cell infiltrate. To the best of our knowledge fewer than 20 cases of cutaneous angioplasmocellular hyperplasia have been published in English literature. We report a case of a 65-year-old man who presented with a long standing asymptomatic flesh colored ulcerated nodule on the back. Histopathological examination revealed a dermal vascular proliferation with polyclonal plasma cell infiltration. A diagnosis of angioplasmocellular hyperplasia was established. This entity is rare and we would like to emphasize the importance of clinico-pathological correlation to differentiate it from various other conditions of cutaneous plasma cell infiltration.
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Dermatol Online J
April 2016
ESIPGIMSR, Basaidarapur, New Delhi.
Angioplasmocellular hyperplasia is a rare clinical condition with blood vessel proliferation and a reactive plasma cell infiltrate. To the best of our knowledge fewer than 20 cases of cutaneous angioplasmocellular hyperplasia have been published in English literature. We report a case of a 65-year-old man who presented with a long standing asymptomatic flesh colored ulcerated nodule on the back.
View Article and Find Full Text PDFJ Am Acad Dermatol
March 2011
Department of Dermatology, Mackay Memorial Hospital, Taipei, Taiwan.
Background: Angioplasmocellular hyperplasia is rarely reported.
Objective: The purpose of this study is to describe and analyze the clinicopathologic features of angioplasmocellular hyperplasia.
Methods: The records of 10 patients (mean age, 45 years; range, 17 to 71 years) with characteristic histologic features of angioplasmocellular hyperplasia were reviewed and the histopathologic findings, clinical features, and medical histories analyzed.
Australas J Dermatol
February 2009
Department of Dermatology, Royal Brisbane Hospital, Queensland, Australia.
Primary cutaneous angioplasmocellular hyperplasia is a plasma-cellular infiltrate that has been reported only once previously in the literature, in a report of a case affecting two Latin American patients. In the present case, a systemically well 62-year-old Caucasian man presented with a nodule on the back of the neck. Histology showed a vascular proliferative process with an abundance of plasma cells in the stroma.
View Article and Find Full Text PDFOral Surg Oral Med Oral Pathol Oral Radiol Endod
February 2000
Department of Oral Surgery, Saitama Medical Center, Saitama Medical School, Kawagoe, Saitama, Japan.
We report a plasma cell granuloma arising in the movable mucosa of the oral cavity of a 50-year-old man. Histologically, the lesion was characterized by a dense nodular infiltrate of mature plasma cells. Immunostaining for kappa and lambda light chains confirmed a polyclonal plasma cell population.
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