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[原发性血小板增多症与胃癌并存]

[Coexistence of essential thrombocythemia and gastric cancer].

作者信息

Kondo H, Sakai Y, Takaso T

机构信息

Department of Medicine, Shimizu Kousei Hospital.

出版信息

Rinsho Ketsueki. 1993 Feb;34(2):224-8.

PMID:8492422
Abstract

A 74-year-old man was admitted because of swelling, pain and ecchymosis in the night lower extremity. A blood analysis revealed that Hb was 11.8g/dl, WBC 37,600/microliters, and platelet count 137.1 x 10(4)/microliters. The NAP value was high. Bone marrow examination disclosed marked megakaryocytic hyperplasia. Chromosomal analysis revealed 47, XY, +9. Hemostatic data were within normal ranges, but the 2nd aggregation of platelet by ADP was diminished. The serum beta-TG was 159, PF-4 56ng/ml, B12 1,100, UB12 BC 1,800pg/ml. Gastric fiberoscopy revealed gastric cancer and CT scan disclosed marked splenomegaly. Essential thrombocythemia (ET) coexisting with gastric cancer was diagnosed based on these examinations. He was treated with anti-platelet agents, busulfan and tegafur uracil, however thromboembolic symptoms suggesting central nervous system and peripheral vascular ischemia and gastrointestinal bleeding occurred. Among diagnostic criteria for ET established by the polycythemia vera study group, there is a category "No known cause for reactive thrombocytosis." The case reported here had gastric cancer which may have contributed to the elevated platelet count, however this case could be diagnosed as ET coexisting with gastric cancer because of the above various clinical signs and laboratory results. Although then are few reports of the coexistence of other malignancies in ET, there may be many more similar cases because of the age preponderance in ET. In order to diagnose ET more precisely, more strict diagnostic criteria are needed.

摘要

一名74岁男性因夜间下肢肿胀、疼痛和瘀斑入院。血液分析显示血红蛋白(Hb)为11.8g/dl,白细胞(WBC)37600/微升,血小板计数137.1×10⁴/微升。中性粒细胞碱性磷酸酶(NAP)值升高。骨髓检查显示巨核细胞明显增生。染色体分析显示为47,XY,+9。止血数据在正常范围内,但二磷酸腺苷(ADP)诱导的血小板二次聚集减少。血清β-血小板球蛋白(β-TG)为159,血小板第4因子(PF-4)56ng/ml,维生素B₁₂ 1100,未结合维生素B₁₂结合物(UB₁₂ BC)1800pg/ml。胃镜检查发现胃癌,计算机断层扫描(CT)显示脾脏明显肿大。根据这些检查诊断为真性红细胞增多症研究组制定的原发性血小板增多症(ET)诊断标准中,有一类是“无已知反应性血小板增多的原因”。本文报道的病例患有胃癌,这可能是血小板计数升高的原因之一,但由于上述各种临床症状和实验室检查结果,该病例可诊断为ET合并胃癌。虽然ET合并其他恶性肿瘤的报道很少,但由于ET患者年龄偏大,可能还有更多类似病例。为了更准确地诊断ET,需要更严格的诊断标准。

相似文献

1
[Coexistence of essential thrombocythemia and gastric cancer].[原发性血小板增多症与胃癌并存]
Rinsho Ketsueki. 1993 Feb;34(2):224-8.
2
Diagnosis of essential thrombocythemia at platelet counts between 400 and 600x10(9)/L. Gruppo Italiano Malattie Mieloproliferative Croniche(GIMMC).血小板计数在400至600×10⁹/L之间时原发性血小板增多症的诊断。意大利慢性骨髓增殖性疾病研究组(GIMMC)
Haematologica. 2000 May;85(5):492-5.
3
Relevance of bone marrow features in the differential diagnosis between essential thrombocythemia and early stage idiopathic myelofibrosis.骨髓特征在原发性血小板增多症与早期特发性骨髓纤维化鉴别诊断中的相关性
Haematologica. 2000 Nov;85(11):1126-34.
4
Essential thrombocythemia in childhood.儿童原发性血小板增多症
Semin Thromb Hemost. 1997;23(3):295-301. doi: 10.1055/s-2007-996102.
5
Clinical and laboratory features, pathobiology of platelet-mediated thrombosis and bleeding complications, and the molecular etiology of essential thrombocythemia and polycythemia vera: therapeutic implications.临床和实验室特征、血小板介导的血栓形成和出血并发症的病理生物学,以及原发性血小板增多症和真性红细胞增多症的分子病因:治疗意义。
Semin Thromb Hemost. 2006 Apr;32(3):174-207. doi: 10.1055/s-2006-939431.
6
Spontaneous megakaryocytic colony formation does not discriminate between essential thrombocythemia and polycythemia vera.
Am J Hematol. 2006 Jul;81(7):554-6. doi: 10.1002/ajh.20592.
7
[Essential thrombocythemia in pregnancy].
Rinsho Ketsueki. 1993 Dec;34(12):1579-83.
8
[Acute megakaryoblastic leukemia developing 11 years after diagnosis of essential thrombocythemia].[原发性血小板增多症诊断11年后发生的急性巨核细胞白血病]
Rinsho Ketsueki. 1991 Aug;32(8):868-73.
9
[Anesthesia in two patients with essential thrombocythemia].[两名原发性血小板增多症患者的麻醉]
Masui. 1997 Nov;46(11):1470-3.
10
[Essential thrombocythemia in transformation to smouldering megakaryoblastic leukemia with myelofibrosis].
Rinsho Ketsueki. 1995 Oct;36(10):1210-6.

引用本文的文献

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Coexistent Breast Cancer and Essential Thrombocythemia: How We Addressed the Therapeutic Challenges.并存的乳腺癌和原发性血小板增多症:我们如何应对治疗挑战。
Case Rep Hematol. 2018 Aug 12;2018:2080185. doi: 10.1155/2018/2080185. eCollection 2018.