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一名患有多种合并症的老年肝硬化患者发生自发性脾梗死。

Spontaneous splenic infarction in an elderly cirrhotic patient with multiple comorbidities.

作者信息

Erarslan Elife, Bozkurt Alper, Yüksel Ilhami, Demır Hanzade Duygu

机构信息

Etlik İhtisas Educational and Research Hospital, Department of Gastroenterology, Ankara, Turkey.

出版信息

Turk J Gastroenterol. 2012;23(5):596-8. doi: 10.4318/tjg.2012.0429.

Abstract

Spontaneous splenic infarction has been seen rarely in cirrhosis and portal hypertension. The clinical presentation can mimic other causes of acute abdominal pain. The diagnosis of the condition is based on clinical findings and splenic imaging. In recent years, ultrasonography and computed tomographic scan have gained in popularity for the diagnosis of splenic infarction. Most reported cases are of focal infarction, and treatment is mostly conservative. Herein, we describe a rare case of spontaneous splenic infarction in an elderly cirrhotic patient with portal hypertension who also had comorbidities. A 72-year-old female previously diagnosed with cirrhosis was admitted for left upper quadrant abdominal pain for two days. Her medical history included cryptogenic cirrhosis, congestive heart failure, chronic obstructive pulmonary disease, and hypertension. Physical examination on admission revealed a palpable splenomegaly. Abdominal ultrasonography revealed splenomegaly and a hypoechoic area with lobulated contours measuring 62 x 35 mm extending from the subcapsular area to the hilus in the middle section of the spleen. Abdominal computed tomographic showed a subcapsular hypodense lesion of the spleen measuring 64 x 58 mm. Doppler ultrasound revealed a wedge-shaped heterogeneous hypoechoic avascular area extending from the central zone to the lateral zone of the spleen. In our case, diagnosis of splenic infarction was made by computed tomographic and Doppler ultrasonography. Our patient received conservative treatment for the underlying diseases. Spontaneous splenic infarction must be kept in mind in cirrhotic patients with underlying comorbidities presenting with left upper quadrant pain.

摘要

自发性脾梗死在肝硬化和门静脉高压症中较为罕见。其临床表现可类似于其他急性腹痛病因。该病的诊断基于临床发现和脾脏影像学检查。近年来,超声检查和计算机断层扫描在脾梗死诊断中的应用越来越广泛。大多数报道的病例为局灶性梗死,治疗多为保守治疗。在此,我们描述一例患有门静脉高压症且伴有多种合并症的老年肝硬化患者发生自发性脾梗死的罕见病例。一名72岁女性,既往诊断为肝硬化,因左上腹疼痛两天入院。她的病史包括隐源性肝硬化、充血性心力衰竭、慢性阻塞性肺疾病和高血压。入院时体格检查发现脾脏可触及肿大。腹部超声检查显示脾脏肿大,脾中部从被膜下区域至脾门有一个轮廓呈分叶状的低回声区,大小为62×35mm。腹部计算机断层扫描显示脾脏有一个64×58mm的被膜下低密度病变。多普勒超声显示一个从脾中央区延伸至外侧区的楔形不均匀低回声无血管区。在我们的病例中,通过计算机断层扫描和多普勒超声检查诊断为脾梗死。我们的患者针对基础疾病接受了保守治疗。对于伴有基础合并症且出现左上腹疼痛的肝硬化患者,必须考虑到自发性脾梗死的可能。

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