Literature DB >> 21422634

Kaposi's sarcoma following immunosuppressive therapy for vasculitis.

Tarik Bouattar1, Laila Kazmouhi, Zaitouna Alhamany, Kawtar Beqqal, Laila Haffane, Tarik Sqalli Houssaini, Hakima Rhou, Loubna Benamar, Karima Senouci, Rabia Bayahia, Naima Ouzeddoun.   

Abstract

Kaposi's sarcoma (KS) is widely reported to develop after renal transplantation and is induced by activation of a latent human herpes virus 8. We report the clinical features and outcome of a 50-year-old woman who presented with KS 18 weeks after starting immunosuppressive therapy for vasculitis. She had positive-titer IgG antibody to human herpes virus 8. Cyclophosphamide pulses were interrupted, and prednisone was decreased gradually to 10 mg/day. Skin lesions showed important regression with stabilization of the general state and renal function. Eight months later, the patient presented with a diffuse cutaneous KS that required the discontinuation of steroids. Within 1 month, her general status and renal function deteriorated, and she died with a disseminated intravascular coagulation syndrome.

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Year:  2011        PMID: 21422634

Source DB:  PubMed          Journal:  Saudi J Kidney Dis Transpl        ISSN: 1319-2442


  3 in total

1.  Kaposi's sarcoma concurrent with granulomatosis polyangiitis.

Authors:  Diler Taş Kılıç; Selma Karaahmetoğlu Özkan; Başol Canbakan; Nesrin Dündar
Journal:  Eur J Rheumatol       Date:  2015-08-21

Review 2.  Kaposi sarcoma in anti-neutrophil cytoplasmic antibody-associated vasculitis: a case-based review.

Authors:  Benedict K Tiong; Arun S Singh; G Peter Sarantopoulos; Tanaz A Kermani
Journal:  Rheumatol Int       Date:  2021-02-23       Impact factor: 2.631

3.  [Kaposi sarcoma complicating aplastic anemia].

Authors:  Mouna Lamchahab; Bouchra Oukkache; Sofia Marouan; Asmae Quessar; Said Benchekroun
Journal:  Pan Afr Med J       Date:  2014-06-19
  3 in total

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