| Literature DB >> 33796182 |
Amel El Korbi1,2, Sondes Jellali1, Mahbouba Jguiri3, Ahlem Bellalah4, Mehdi Ferjaoui1, Rachida Bouatay1, Naourez Kolsi1,2, Khaled Harrathi1, Jamel Koubaa1.
Abstract
Castleman's disease is a rare pathology, poorly understood. It is considered as a lymphoproliferative disorder, described for the first time in 1954, which may be confused with other causes of lymphadenopathy. We report in this paper the case of a young women presenting with left latero-cervical lymphadenopathy. All the investigations were negative except a large high-vascularized level II cervical lymphadenopathy. We performed a cervicotomy. The extemporaneous histological exam was non-contributive. We decided to perform a complete level II and III left cervical lymphadenectomy. The diagnosis of unicentric Castleman's disease was confirmed based on the final histological study of the specimen, and the absence of other cervical and extra-cervical lymphadenopathy. The patient is free of recurrence at the time of reporting this article. Copyright: Amel El Korbi et al.Entities:
Keywords: Castleman’s disease; lymphadenopathy; surgery
Mesh:
Year: 2020 PMID: 33796182 PMCID: PMC7992414 DOI: 10.11604/pamj.2020.37.369.26909
Source DB: PubMed Journal: Pan Afr Med J