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镰状细胞贫血患儿的巨大脾梗死及脾切除术的作用

Massive splenic infarction in children with sickle cell anemia and the role of splenectomy.

作者信息

Al-Salem Ahmed H

机构信息

Department of Pediatric Surgery, Maternity and Children Hospital, Dammam, Saudi Arabia.

出版信息

Pediatr Surg Int. 2013 Mar;29(3):281-5. doi: 10.1007/s00383-012-3223-2. Epub 2012 Nov 27.

Abstract

BACKGROUND

Massive splenic infarction (MSI) is a very rare condition. Few reports of splenic infarction of various etiologies including hematological and non-hematological causes have been published. On the other hand, MSI in patients with sickle cell anemia (SCA) is extremely rare. This report describes our experience with 15 children with SCA and MSI outlining aspects of presentation, diagnosis and management.

PATIENTS AND METHODS

The records of all children with MSI were retrospectively reviewed for age at diagnosis, sex, clinical features, precipitating factors, investigations, management and outcome.

RESULTS

15 children (11 M: 4 F) with SCA were treated for MSI. Their mean age was 10.9 years (6-17 years). All presented with severe left upper quadrant abdominal pain. In nine, this was associated with nausea and vomiting. Three were febrile and all had a tender splenomegaly. Their mean hemoglobin was 8.2 g/dl (5.7-11.3 g/dl), mean WBC was 10.97 × 10(3) mm(-3) (3.6 × 10(3)-22.3 × 10(3) mm(-3)) and mean platelet count was 263.3 × 10(3) mm(-3) (40 × 10(3)-660 × 10(3) mm(-3)). In seven, there was a precipitating cause including high altitude in two, acute chest syndrome in two, septicemia in two and severe vasooclusive crisis in one. Abdominal ultrasound and CT scan confirmed the diagnosis of MSI which involved more than half of the spleen in 12 and whole spleen in 3. All were treated with IV fluids, analgesia and blood transfusion where appropriate. Eleven had splenectomy because of persistent abdominal pain, three developed splenic abscess and underwent splenectomy and one settled on conservative treatment. Histology confirmed the diagnosis of splenic infarction in 11 and infarction with abscess in the remaining 3.

CONCLUSION

MSI is extremely rare in children with SCA. It can develop spontaneously or precipitated by other factors namely high altitude, acute chest syndrome and severe stress. Most reported cases of splenic infarction are small in size, focal and can be treated conservatively. MSI, on the other hand, may necessitate splenectomy for persistent symptoms or in case of complications, such as abscess formation.

摘要

背景

大面积脾梗死(MSI)是一种非常罕见的病症。关于包括血液学和非血液学病因在内的各种病因导致的脾梗死的报道很少。另一方面,镰状细胞贫血(SCA)患者发生MSI极为罕见。本报告描述了我们对15例患有SCA和MSI的儿童的治疗经验,概述了其临床表现、诊断和治疗方面。

患者与方法

对所有患有MSI的儿童的记录进行回顾性分析,包括诊断时的年龄、性别、临床特征、诱发因素、检查、治疗及预后。

结果

15例患有SCA的儿童接受了MSI治疗。他们的平均年龄为10.9岁(6 - 17岁)。所有患儿均表现为左上腹剧痛。其中9例伴有恶心和呕吐。3例发热,所有患儿脾脏均有压痛且肿大。他们的平均血红蛋白为8.2 g/dl(5.7 - 11.3 g/dl),平均白细胞计数为10.97×10³/mm³(3.6×10³ - 22.3×10³/mm³),平均血小板计数为263.3×10³/mm³(40×10³ - 660×10³/mm³)。7例有诱发因素,其中2例为高原反应,2例为急性胸部综合征,2例为败血症,1例为严重血管闭塞性危机。腹部超声和CT扫描确诊为MSI,其中12例梗死面积超过脾脏一半,3例整个脾脏梗死。所有患儿均接受了静脉补液、镇痛治疗,并在必要时进行了输血。11例因持续性腹痛接受了脾切除术,3例发生脾脓肿并接受了脾切除术,1例采用保守治疗后病情缓解。组织学检查证实11例为脾梗死,其余3例为梗死合并脓肿。

结论

MSI在SCA儿童中极为罕见。它可自发发生或由其他因素诱发,如高原反应、急性胸部综合征和严重应激。大多数报道的脾梗死病例面积小、呈局灶性,可采用保守治疗。另一方面,MSI可能因持续症状或出现并发症(如脓肿形成)而需要进行脾切除术。

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