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遗传性球形红细胞增多症:脾切除患者的研究

Hereditary spherocytosis: a study of splenectomized persons.

作者信息

Schilling R F

出版信息

Semin Hematol. 1976 Jul;13(3):169-76.

PMID:935888
Abstract

Sixty-one persons splenectomized for hereditary spherocytosis have been studied and compared to 36 nonsplenectomized clinically affected and to 77 nonaffected family members. Serum IgM levels were reduced by 25% and IgD levels were nearly doubled in the splenectomized group. No fatal bacterial infection was identified by history covering a total of 800 postsplenectomy years. Platelet counts remained elevated for many years after removal of the spleen, as did the number of leukocytes, lymphocytes, and monocytes. Heinz bodies were seen in 3% of red cells after splenectomy. Though within the range of "normal," reticulocyte levels and serum bilirubin levels were satistically higher in the splenectomized group than in the nonaffected persons. Hemoglobin levels were higher in splenectomized affected persons than in matched controls of the same sex and maturity.

摘要

对61例因遗传性球形红细胞增多症而行脾切除术的患者进行了研究,并与36例有临床症状但未行脾切除术的患者以及77例未受影响的家庭成员进行了比较。脾切除组的血清IgM水平降低了25%,IgD水平几乎翻倍。在涵盖总共800个脾切除术后年份的病史中,未发现致命的细菌感染。脾切除后,血小板计数多年来一直升高,白细胞、淋巴细胞和单核细胞的数量也是如此。脾切除术后,3%的红细胞中可见海因茨小体。尽管在“正常”范围内,但脾切除组的网织红细胞水平和血清胆红素水平在统计学上高于未受影响的人群。脾切除术后受影响的患者血红蛋白水平高于相同性别和成熟度的匹配对照组。

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1
Hereditary spherocytosis: a study of splenectomized persons.遗传性球形红细胞增多症:脾切除患者的研究
Semin Hematol. 1976 Jul;13(3):169-76.
2
Red cell life span after splenectomy in hereditary spherocytosis.遗传性球形红细胞增多症脾切除术后的红细胞寿命
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[Familial hereditary spherocytosis in the pediatric patient].[小儿患者的家族性遗传性球形红细胞增多症]
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[Erythrocyte metabolism before and after splenectomy in hereditary spherocytosis].[遗传性球形红细胞增多症脾切除术前及术后的红细胞代谢]
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Pitted erythrocytes in splenectomized subjects with congenital spherocytosis and in subjects splenectomized for other reasons.患有先天性球形红细胞增多症的脾切除患者以及因其他原因行脾切除术的患者中的凹陷红细胞。
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Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia.膜丢失的时间差异导致遗传性球形红细胞增多症和免疫性溶血性贫血中出现不同的网织红细胞特征。
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Oxygen affinity and compensated hemolysis in hereditary spherocytosis.遗传性球形红细胞增多症中的氧亲和力与代偿性溶血
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Medicine (Baltimore). 2015 Mar;94(9):e610. doi: 10.1097/MD.0000000000000610.
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Laparoscopic versus robotic subtotal splenectomy in hereditary spherocytosis. Potential advantages and limits of an expensive approach.腹腔镜与机器人辅助部分脾切除术治疗遗传性球形红细胞增多症:一种昂贵方法的潜在优势和局限性。
Surg Endosc. 2012 Oct;26(10):2802-9. doi: 10.1007/s00464-012-2249-9. Epub 2012 Apr 5.
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Contemporary pediatric splenectomy: continuing controversies.
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Pediatr Surg Int. 2011 Nov;27(11):1165-71. doi: 10.1007/s00383-011-2929-x. Epub 2011 May 28.
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Traditional laboratory measures of cardiovascular risk in hereditary spherocytosis.遗传性球形红细胞增多症的传统心血管风险实验室检测指标。
Pediatr Blood Cancer. 2010 Oct;55(4):684-9. doi: 10.1002/pbc.22640.
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Vascular complications after splenectomy for hematologic disorders.血液系统疾病脾切除术后的血管并发症。
Blood. 2009 Oct 1;114(14):2861-8. doi: 10.1182/blood-2009-04-210112. Epub 2009 Jul 27.
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Laparoscopic partial splenectomy: indications and results of a multicenter retrospective study.腹腔镜下部分脾切除术:一项多中心回顾性研究的适应症及结果
Surg Endosc. 2008 Jan;22(1):45-9. doi: 10.1007/s00464-007-9509-0. Epub 2007 Oct 18.
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Clinical and hematologic benefits of partial splenectomy for congenital hemolytic anemias in children.儿童先天性溶血性贫血行部分脾切除术的临床及血液学益处。
Ann Surg. 2003 Feb;237(2):281-8. doi: 10.1097/01.SLA.0000048453.61168.8F.
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Clinicopathologic features of young and old sphha/sphha mice. Mutants with congenital hemolytic anemia.年轻和年老的sphha/sphha小鼠的临床病理特征。患有先天性溶血性贫血的突变体。
Am J Pathol. 1988 Sep;132(3):461-73.
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Ann Surg. 1987 Jan;205(1):13-7. doi: 10.1097/00000658-198701000-00003.
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Hereditary spherocytosis revisited. Eighth annual Paul M. Aggeler Memorial Lecture. Delivered October 25, 1977, San Francisco General Hospital Medical Center.再探遗传性球形红细胞增多症。第八届年度保罗·M·阿格勒纪念讲座。于1977年10月25日在旧金山综合医院医疗中心发表。
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