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脾脏自发性破裂作为套细胞淋巴瘤母细胞样变异型的首发表现。

Spontaneous rupture of the spleen as the presenting feature of the blastoid variant of mantle cell lymphoma.

作者信息

Mason K D, Juneja S K

机构信息

Department of Diagnostic Haematology, Royal Melbourne Hospital, Victoria, Australia.

出版信息

Clin Lab Haematol. 2003 Aug;25(4):263-5. doi: 10.1046/j.1365-2257.2003.00522.x.

DOI:10.1046/j.1365-2257.2003.00522.x
PMID:12890168
Abstract

Spontaneous splenic rupture is rare, and particularly so as the initial presentation of a lymphoproliferative disorder. Although rare cases of splenic rupture have been reported in mantle cell lymphoma there has not been a report of the blastoid variant presenting in this manner. We report such a case in a 64-year-old man.

摘要

自发性脾破裂很少见,尤其是作为淋巴增殖性疾病的首发表现。虽然已有报道套细胞淋巴瘤中存在罕见的脾破裂病例,但尚未有母细胞样变异型以这种方式出现的报道。我们报告了一名64岁男性的此类病例。

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Spontaneous rupture of the spleen as the presenting feature of the blastoid variant of mantle cell lymphoma.脾脏自发性破裂作为套细胞淋巴瘤母细胞样变异型的首发表现。
Clin Lab Haematol. 2003 Aug;25(4):263-5. doi: 10.1046/j.1365-2257.2003.00522.x.
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