Literature DB >> 32581162

Iatrogenic Penile Kaposi Sarcoma.

Satoshi Akao1, Hiroyuki Yano2, Mitsuyo Kinjo2.   

Abstract

Entities:  

Keywords:  iatrogenic; immunosuppression; kaposi sarcoma

Year:  2020        PMID: 32581162      PMCID: PMC7644506          DOI: 10.2169/internalmedicine.4751-20

Source DB:  PubMed          Journal:  Intern Med        ISSN: 0918-2918            Impact factor:   1.271


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A 78-year-old man presented with a growing painless penile nodule one month after receiving prednisolone 60 mg daily and intravenous cyclophosphamide 500 mg for ANCA (anti-neutrophil cytoplasmic antibody) associated vasculitis. Physical examination revealed a non-tender reddish nodule measuring 3 cm in diameter on the glans (Picture 1), without any other lesions. HIV (human immunodeficiency virus) antigen and HTLV-1 (human T-lymphotropic virus type I) antibody tests were negative. A biopsy of the lesion showed the presence of spindle cells replacing dermal collagen, vascular spaces containing red blood cells, extravasated red blood cells, and hemosiderin in macrophages, thus leading to a diagnosis of Kaposi sarcoma (Picture 2). The nodule gradually shrunk over three months after tapering prednisolone to 10 mg and applying imiquimod ointment.
Picture 1.
Picture 2.
Kaposi sarcoma has five epidemiological forms; acquired immunodeficiency syndrome-related, iatrogenic, endemic, classic, and homosexual men without HIV infection. Iatrogenic Kaposi sarcoma usually develops following a solid organ allograft and it is rarely seen in non-transplant patients undergoing immunosuppressive therapy. Iatrogenic Kaposi sarcoma generally regresses after tapering immunosuppressive treatments (1,2). The authors state that they have no Conflict of Interest (COI).
  2 in total

Review 1.  Kaposi sarcoma.

Authors:  Ethel Cesarman; Blossom Damania; Susan E Krown; Jeffrey Martin; Mark Bower; Denise Whitby
Journal:  Nat Rev Dis Primers       Date:  2019-01-31       Impact factor: 52.329

2.  Iatrogenic Kaposi's sarcoma after immunosuppressive treatment for granulomatosis with polyangiitis (Wegener's).

Authors:  Anjali Saxena; Elena Netchiporouk; Raqiya Al-Rajaibi; Robin Billick; Osama Roshdy
Journal:  JAAD Case Rep       Date:  2015-03-06
  2 in total

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