Sueyoshi Yuka, Yoshio Toshiyuki, Ito Mari, Suemura Shigeki, Araki Manabu, Mitsuta Chiaki, Ota Makiyo, Ohta Takashi, Hasegawa Hiroko, Tatsumi Kaori, Toyama Takashi, Nakazuru Shoichi, Kuzushita Noriyoshi, Tsujie Masanori, Miyamoto Atsushi, Nakamori Shoji, Kodama Yoshinori, Mita Eiji
Department of Gastroenterology and Hepatology, Osaka National Hospital, 2-1-14 Houenzaka, Chuo-ku, Osaka, Osaka, 540-0006, Japan.
Department of Surgery, Osaka National Hospital, Osaka, Japan.
Clin J Gastroenterol. 2012 Feb;5(1):42-6. doi: 10.1007/s12328-011-0272-3. Epub 2011 Dec 22.
Spontaneous splenic rupture is a life-threatening disease and an important differential diagnosis of acute abdomen. Early clinical diagnosis and rapid intervention is required to ensure patient survival. Spontaneous splenic rupture may be induced by hematological, inflammatory or infiltrative diseases affecting the spleen. Splenomegaly may also significantly increase the risk of rupture. Other contributory factors include male, adulthood, rapid growth of the spleen and splenic abscess. Here, we present the case of a 69-year-old man who was undergoing chemotherapy for B-cell chronic lymphoid leukemia. He was admitted to our hospital after he suddenly developed persistent upper abdominal pain. Computed tomography and ultrasonography revealed accumulation of free fluid in and around the spleen. He was diagnosed as having spontaneous splenic rupture and an emergency operation was performed. During the operation, we found a massively enlarged spleen with several capsular tears, and performed a splenectomy. The patient made a good recovery. Pathological examination revealed that the spleen was infiltrated by CD20-, CD5- and CD23-positive lymphoid blasts. We encountered a case of spontaneous splenic rupture in a patient receiving chemotherapy for exacerbating B-cell chronic lymphoid leukemia. In a case of abdominal pain of acute onset in patients with hematological disease, spontaneous splenic rupture should be suspected.
自发性脾破裂是一种危及生命的疾病,也是急性腹痛的重要鉴别诊断。需要早期临床诊断和快速干预以确保患者存活。自发性脾破裂可能由影响脾脏的血液学、炎症性或浸润性疾病引起。脾肿大也可能显著增加破裂风险。其他促成因素包括男性、成年、脾脏快速生长和脾脓肿。在此,我们报告一例69岁男性患者,他正在接受B细胞慢性淋巴细胞白血病化疗。他在突然出现持续上腹部疼痛后入院。计算机断层扫描和超声检查显示脾脏内及周围有游离液体积聚。他被诊断为自发性脾破裂并接受了急诊手术。手术中,我们发现脾脏巨大肿大,有多处包膜撕裂,并进行了脾切除术。患者恢复良好。病理检查显示脾脏被CD20、CD5和CD23阳性的淋巴母细胞浸润。我们遇到一例因B细胞慢性淋巴细胞白血病病情加重而接受化疗的患者发生自发性脾破裂。对于血液系统疾病患者急性发作的腹痛病例,应怀疑自发性脾破裂。