Kaposi’s Sarcoma in HIV Positive Male

Authors

  • Mohammad Emrul Hasan Khan Assistant Registrar, Burn Plastic & Reconstructive Surgery Dept. Shaheed Suhrawardi Medical College Hospital, Dhaka
  • Masum Parvag Medical Officer, Plastic & Reconstructive Surgery Dept. Shaheed Suhrawardi Medical College Hospital, Dhaka
  • Mahabub Alam Assistant Registrar, Burn Plastic & Reconstructive Surgery Dept. Shaheed Suhrawardi Medical College Hospital, Dhaka
  • Shaon Shahriar Assistant Registrar, Burn Plastic & Reconstructive Surgery Dept. Shaheed Suhrawardi Medical College Hospital, DHaka
  • Ahmad Seraji Assistant Professor, Burn Plastic & Reconstructive Surgery Dept. Shaheed Suhrawardi Medical College Hospital, Dhaka
  • Md Shahidul Bari Professor & Head of the Dept. Burn Plastic & Reconstructive Surgery Dept. Shaheed Suhrawardi Medical College Hospital, Dhaka

DOI:

https://doi.org/10.3329/jbcps.v32i3.26055

Keywords:

HIV infection, Kaposi’s sarcoma

Abstract

Kaposis sarcoma is a vascular tumor usually involves skin, mucous membrane and other organs. HIV associated Kaposis sarcoma is very rarely reported in Bangladesh. The reporting case was presented with a recurrent, ulcerated, firm nodule on left groin along with multiple blackish flat or raised lesions on different parts of body. According to previous histopathological report this case was operated as a case of recurrent fibrous histiocytoma and this time the diagnosis was confirmed histologically and by immunohistochemistry as Kaposis sarcoma. Later, it was found that the patient is serologically positive for HIV.

J Bangladesh Coll Phys Surg 2014; 32: 164-166

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Author Biography

Mohammad Emrul Hasan Khan, Assistant Registrar, Burn Plastic & Reconstructive Surgery Dept. Shaheed Suhrawardi Medical College Hospital, Dhaka



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Published

2015-12-23

How to Cite

Khan, M. E. H., Parvag, M., Alam, M., Shahriar, S., Seraji, A., & Bari, M. S. (2015). Kaposi’s Sarcoma in HIV Positive Male. Journal of Bangladesh College of Physicians and Surgeons, 32(3), 164–166. https://doi.org/10.3329/jbcps.v32i3.26055

Issue

Vol. 32 No. 3 (2014)

Section

Case Reports

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