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骨髓移植后复发性霍奇金病

Recurrent Hodgkin's disease after bone marrow transplantation.

作者信息

Shahab I, Greer J P, Beeker T A, Wolff S N, Collins R D, Cousar J B

机构信息

Department of Pathology, Vanderbilt University Medical Center, Nashville, Tennessee 37232-5310, USA.

出版信息

Am J Clin Pathol. 1997 Jan;107(1):74-80. doi: 10.1093/ajcp/107.1.74.

DOI:10.1093/ajcp/107.1.74
PMID:8980371
Abstract

Histologic features of recurrent Hodgkin's disease (HD) after conventional therapy are well known, but few studies describe HD after bone marrow transplantation (BMT). Histologic material from 63 patients who underwent BMT performed to treat recurrent nodular sclerosing HD (NSHD) between 1985 and 1994 was examined; 13 of the 63 patients had histologically proved recurrent disease after BMT. Histologic material and clinical findings from the original diagnostic biopsy specimen and pre-BMT and post-BMT specimens were available from our study population of eight patients (five male, three female; age range, 16 to 38 years; median age, 27.5 years). Seven patients had recurrent NSHD after BMT; sites of recurrence included lymph nodes only (four patients), and lymph nodes and lung, lung and liver, and lung only (one patient each). In one patient, a high-grade non-Hodgkin's B-cell lymphoma developed in the large intestine 5 years after BMT. In another, disease progressed from grade 1 in the original biopsy specimen to grade 2 in both the pre-BMT and post-BMT recurrent HD biopsy specimens. Post-BMT biopsy specimens of recurrent HD with lung involvement revealed a substantial increase in sclerosis and fibroblastic features. Paraffin immunoperoxidase studies in seven patients demonstrated substantial change in phenotype of Reed-Stemberg cell variants in only one post-BMT recurrent HD specimen, which showed a +2 reaction with CD30 (Ki-1). No substantial differences in the reactive component were noted between the original biopsy specimen and pre-BMT and post-BMT specimens of recurrent disease. In summary, histologic findings of post-BMT recurrent NSHD do not differ significantly from those of the original diagnostic biopsy or pre-BMT recurrent HD specimens. The lung is the most common site of extranodal post-BMT recurrence. In one patient, high-grade non-Hodgkin's B-cell lymphoma developed after BMT performed to treat recurrent HD.

摘要

常规治疗后复发性霍奇金病(HD)的组织学特征已为人熟知,但很少有研究描述骨髓移植(BMT)后的HD情况。对1985年至1994年间接受BMT治疗复发性结节硬化型HD(NSHD)的63例患者的组织学材料进行了检查;63例患者中有13例在BMT后经组织学证实有复发性疾病。我们的8例患者(5例男性,3例女性;年龄范围16至38岁;中位年龄27.5岁)的研究群体可获得原始诊断活检标本、BMT前和BMT后的标本的组织学材料及临床发现。7例患者在BMT后出现复发性NSHD;复发部位仅包括淋巴结(4例患者),以及淋巴结和肺、肺和肝、仅肺(各1例患者)。1例患者在BMT后5年大肠发生了高级别非霍奇金B细胞淋巴瘤。另1例患者,疾病从原始活检标本中的1级进展为BMT前和BMT后复发性HD活检标本中的2级。伴有肺部受累的复发性HD的BMT后活检标本显示硬化和纤维母细胞特征显著增加。7例患者的石蜡免疫过氧化物酶研究仅在1例BMT后复发性HD标本中显示里德-斯腾伯格细胞变体的表型有显著变化,该标本对CD30(Ki-1)呈+2反应。在复发性疾病的原始活检标本与BMT前和BMT后的标本之间,未观察到反应成分有显著差异。总之,BMT后复发性NSHD的组织学发现与原始诊断活检或BMT前复发性HD标本的组织学发现无显著差异。肺是BMT后结外复发最常见的部位。1例患者在接受BMT治疗复发性HD后发生了高级别非霍奇金B细胞淋巴瘤。

相似文献

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Recurrent Hodgkin's disease after bone marrow transplantation.骨髓移植后复发性霍奇金病
Am J Clin Pathol. 1997 Jan;107(1):74-80. doi: 10.1093/ajcp/107.1.74.
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Composite lymphoma. A clinicopathologic analysis of nine patients with Hodgkin's disease and B-cell non-Hodgkin's lymphoma.复合性淋巴瘤。9例霍奇金病合并B细胞非霍奇金淋巴瘤患者的临床病理分析。
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Cutaneous Hodgkin's disease: an immunohistochemical analysis.皮肤霍奇金淋巴瘤:免疫组织化学分析
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Primary mediastinal large B-cell lymphoma: a comparative study with nodular sclerosis-type Hodgkin's disease.原发性纵隔大B细胞淋巴瘤:与结节硬化型霍奇金病的对比研究。
Int J Hematol. 2001 Aug;74(2):178-85. doi: 10.1007/BF02982002.
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[Hodgkin's and Reed-Sternberg cells in the peripheral blood of a patient with advanced stage Hodgkin's disease].[晚期霍奇金病患者外周血中的霍奇金和里德-斯腾伯格细胞]
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Cutaneous CD30 (Ki-1)-positive anaplastic large cell lymphoma preceded by Hodgkin's disease.霍奇金病之前出现的皮肤CD30(Ki-1)阳性间变性大细胞淋巴瘤。
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Allogeneic bone marrow transplantation for relapsed and refractory Hodgkin's disease and non-Hodgkin's lymphoma.异基因骨髓移植治疗复发难治性霍奇金淋巴瘤和非霍奇金淋巴瘤。
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Extranodal lymphocyte predominance Hodgkin's disease. Clinical and pathologic features.结外淋巴细胞为主型霍奇金淋巴瘤。临床及病理特征。
Am J Clin Pathol. 1995 Apr;103(4):485-91. doi: 10.1093/ajcp/103.4.485.

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