AI Article Synopsis

  • Castleman's disease is a rare condition marked by various clinical symptoms and unique tissue changes, with unclear causes and connections to factors like HIV and human herpesvirus-8.
  • The disease can be localized or multifocal, where the latter can lead to severe health issues, primarily affecting HIV-positive or immunocompromised individuals.
  • The report details two cases diagnosed with Castleman's disease through histopathology and immunohistochemical testing, successfully treated with surgery or rituximab, resulting in symptom-free follow-ups.

Article Abstract

Castleman's disease is a rare lympho-proliferative disease entity characterized by variable clinical presentations, distinctive histological manifestations, and prognosis. Its incidence and etiology are unclear. An interplay of HIV and human herpesvirus-8 has been implicated. Although its localized variety is benign, other types can be multifocal with adverse systemic manifestations. Human herpesvirus-8 Castleman's disease affects mainly HIV-positive individuals; however, individuals who are immunocompromised from other causes can also be affected, thus necessitating investigations for HIV. Herein, we report two patients presenting with long-standing lymphadenopathy. Histopathology, immunohistochemical testing and clinico-pathological correlation confirmed the diagnosis of Castleman's disease. The patients were successfully treated with surgery and/or rituximab. They were symptoms free in the subsequent follow-up visits. A brief review of the literature is also provided.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10214097PMC
http://dx.doi.org/10.1177/2050313X231175720DOI Listing

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