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Sarcoidosis presenting as massive splenomegaly and severe epistaxis case report

机译:结节病表现为大量脾肿大和严重鼻epi病例报告

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摘要

Sarcoidosis is a multisystem disorder of unknown etiology. Extrapulmonary sarcoidosis can involve any organ, but isolated spleen involvement is rare. Diagnosis can be challenging as other etiologies may have similar presentations. A 58-year-old African American female presented with life threatening epistaxis, anemia, refractory thrombocytopenia, and massive splenomegaly. Lymphoproliferative, infectious, and autoimmune etiologies were eliminated with laboratory testing and bone marrow biopsy. The patient had multiple splenic artery aneurysms precluding an open diagnostic splenectomy. Partial splenic artery embolization was performed, which normalized the platelet count and resolved the spontaneous bleeding. This allowed diagnostic splenectomy and splenic artery repair to be safely performed. Surgical pathology demonstrated extensive non-caseating granulomas consistent with sarcoidosis. We present this case to demonstrate the omnipotent nature of sarcoidosis and a complex multi-disciplinary approach for successful diagnosis and treatment.
机译:结节病是病因未知的多系统疾病。肺外结节病可累及任何器官,但很少有脾脏受累。由于其他病因可能具有相似的表现,因此诊断可能具有挑战性。一名58岁的非洲裔美国女性,表现出威胁生命的鼻axis,贫血,难治性血小板减少症和大量脾肿大。实验室检测和骨髓活检消除了淋巴增生,感染和自身免疫性病因。该患者有多发性脾动脉瘤,排除了开放性诊断性脾切除术。进行部分脾动脉栓塞术,使血小板计数正常化并解决了自发性出血。这样可以安全地进行诊断性脾切除术和脾动脉修复。手术病理证实与结节病一致的广泛性非干酪性肉芽肿。我们目前的情况表明结节病的无所不能的性质和成功诊断和治疗的复杂的多学科方法。

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