Mohan Anant, Sood Rita, Shariff Nasir, Gulati Manpreet Singh, Gupta Siddharth Datta, Dutta Amit Kumar
Department of Medicine, All India Institute of Medical Sciences, Ansari Nagar, New Delhi.
Am J Med Sci. 2004 Sep;328(3):170-2. doi: 10.1097/00000441-200409000-00007.
Sarcoidosis is a multisystemic granulomatous disease of unknown origin occurring worldwide and affecting people of all races and ages. This disease manifests most frequently with bilateral hilar lymphadenopathy, pulmonary infiltrates, and skin and ocular lesions. Granulomatous inflammation of the spleen is common in patients with sarcoidosis, but splenic enlargement is unusual and massive splenomegaly quite rare. Splenomegaly is usually homogeneous, but multiple low-attenuating nodular lesions are occasionally seen and easily mistaken for lymphoma, metastases, or infections such as tuberculosis. We describe an unusual case of sarcoidosis in a woman who presented with massive splenomegaly with extensive nodularity that cleared completely with corticosteroid therapy.
结节病是一种病因不明的多系统肉芽肿性疾病,在全球范围内均有发生,影响所有种族和年龄段的人群。这种疾病最常表现为双侧肺门淋巴结肿大、肺部浸润以及皮肤和眼部病变。结节病患者中脾脏出现肉芽肿性炎症很常见,但脾肿大并不常见,巨大脾肿大则极为罕见。脾肿大通常是均匀性的,但偶尔可见多个低密度结节性病变,容易被误诊为淋巴瘤、转移瘤或结核病等感染性疾病。我们报告一例不寻常的结节病病例,患者为一名女性,表现为伴有广泛结节的巨大脾肿大,经皮质类固醇治疗后完全消退。