[Hepatosplenic sarcoidosis: description of a case at the University hospital center of Brazzaville, Congo].

Medecine tropicale et sante internationale Pub Date : 2024-02-05 eCollection Date: 2024-03-31 DOI:10.48327/mtsi.v4i1.2024.478
Alexis Elira Dokekias, M R Adegbinni Akande, Firmine Olivia Galiba Atipotsiba, Lydie Ocini Ngolet, Richard Mikouiyi Ngoulou, Jennifer Elira Samba, Didace Massamba Miabaou, Donatien Moukassa
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Abstract

Sarcoidosis is a multisystem inflammatory disease of unknown etiology. The isolated extrapulmonary form is rare. We report the case of hepatosplenic sarcoidosis in a 29-year-old female patient.It is a patient with no notable medical history, who was seen in consultation for repeated epistaxis. Clinical examination noted nodular hepatomegaly associated with signs of portal hypertension and splenomegaly. Sedimentation rate, alkaline phosphatase, serum angiotensin converting enzyme, aminotransferases were high. Histological examination of the spleen and liver biopsy noted granulomatous inflammatory infiltration without cancerous lesion or tonsil stones.This picture is comparable with sarcoidosis, despite the absence of PET scans. The main challenge remains the differential diagnosis with other granulomatoses. Corticosteroid therapy is the first-line treatment, and after splenectomy the patient has achieved clinical and biological stability.

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[肝脾肉瘤病:刚果布拉柴维尔大学医院中心的病例描述]。
肉样瘤病是一种病因不明的多系统炎症性疾病。孤立的肺外病变非常罕见。我们报告了一例 29 岁女性患者的肝脾肉样肿大病。该患者无明显病史,因反复鼻衄就诊。临床检查发现肝脏结节性肿大,伴有门脉高压和脾脏肿大。血沉、碱性磷酸酶、血清血管紧张素转换酶和转氨酶均偏高。脾脏和肝脏活检组织学检查发现有肉芽肿性炎性浸润,但无癌症病变或扁桃体结石。主要的挑战仍然是与其他肉芽肿病的鉴别诊断。皮质类固醇疗法是一线治疗方法,脾脏切除术后,患者的临床和生物学状态均趋于稳定。
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