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Spontaneously regressed Kaposi’s sarcoma and human herpesvirus 8 infection in a human immunodeficiency virus‐negative patient
Author(s) -
Kondo Yasuko,
Izumi Tatsuya,
Yanagawa Tatsuo,
Kanda Hiroaki,
Katano Harutaka,
Sata Tetsutaro
Publication year - 2000
Publication title -
pathology international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.73
H-Index - 74
eISSN - 1440-1827
pISSN - 1320-5463
DOI - 10.1046/j.1440-1827.2000.01043.x
Subject(s) - sarcoma , medicine , pathology , kaposi's sarcoma , biopsy , immunosuppression , skin biopsy , immunohistochemistry , serology , antibody , immunology , human herpesvirus
Kaposi’s sarcoma occurring in a 78‐year‐old woman, with the absence of the human immunodeficiency virus infection, was correctly diagnosed by immunohistochemistry using anti‐human herpesvirus 8 (HHV8) antibody (PA1‐73N) for the first time. The patient suffered from chronic respiratory failure and was treated with a low dose of steroids for 2.5 years. After her medication dosage was increased for the exacerbation of the respiratory failure, multiple skin tumors in her feet and legs suddenly developed. Histopathologically, skin tumors were suspected as Kaposi’s sarcoma at the first biopsy and reactive angiomatosis at the second biopsy. Polymerase chain reaction and immunohistochemistry, however, revealed the presence of HHV8 DNA fragment and positive staining in the majority of spindle cells in the skin tumors. Serological examination confirmed the positivity of anti‐HHV8 antibodies. HHV8 infection and steroid‐induced immunosuppression, as well as environmental factors played a role in the development of Kaposi’s sarcoma in this patient, because she was born in Okinawa, which is a well‐known endemic area of Kaposi’s sarcoma in Japan. As her general condition improved, the skin lesions regressed without any specific treatment, and disappeared completely 8 months later, in which regression may be associated with evidence of numerous CD8 cell infiltration in the second biopsy tissues. No recurrence was observed during the following 6 month follow up.

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