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Назив: Splenomegaly in sarcoidosis: Frequency, treatment, prognosis and long-term follow-up
Аутори: Zora Pavlović Popović 
Bojan Zarić 
Zdravko Kosjerina
Dragana Petrović
Кључне речи: sarcoidosis;clinical characteristics;splenomegaly
Датум издавања: 1-јан-2015
Часопис: Srpski Arhiv za Celokupno Lekarstvo
Сажетак: © 2015, Serbia Medical Society. Introduction The splenic involvement is common in sarcoidosis, but its real frequency is still obscure, depending doubtless on the method of splenomegaly detection. Splenomegaly may be accompanied with pain or anemia, leucopenia and thrombocytopenia. Objective The aim of this study was to investigate the frequency of splenomegaly related to clinical characteristics of sarcoidosis and to solve the dilemma – whether to introduce medicaments, and when to perform splenectomy. Methods The method of the study is a retrospective and prospective analysis of the patients’ material. Results The study included 540 patients with sarcoidosis in a 20-year period. Of them, 26% had splenomegaly detected by computerized tomography screening. Splenomegaly was more frequently registered in the patients with a longer history of sarcoidosis (38%), as compared to those with a shorter history of the disease (23%) (p<0.05). Splenomegaly was more frequently registered in the patients with other extrapulmonary lesions detected (33%) than in those who had no extrapulmonary manifestations of sarcoidosis (17%) (p<0.01). Indications, possible benefits and complications of splenectomy were analysed in 11 sarcoidosis patients undergoing this intervention for various reasons, of which the follow-up period ranged from one to 20 years. Conclusion Splenomegaly was more frequent in chronic cases or in the patients with established sarcoid lesions of other extrapulmonary organs. The primary treatment of uncomplicated symptomatic splenic sarcoidosis includes medicamentous therapy. Occasionally, splenectomy is required. Prognostically, splenomegaly indicates an unfavorable course of the disease.
URI: https://open.uns.ac.rs/handle/123456789/6619
ISSN: 3708179
DOI: 10.2298/SARH1506279P
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