Synchronous brain and intravascular B-cell lymphoma after remission of an adult hemophagocytic syndrome

被引：3

作者：

Fonseca, Valter R. ^{[1
,2
]}

Espada, Eduardo ^{[2
,3
]}

Geraldes, Ruth ^{[2
,4
]}

Ortiz, Santiago ^{[5
]}

Sousa, Rita ^{[6
]}

Lopez, Dolores ^{[5
]}

Silva, Marisa Teixeira ^{[1
]}

Victorino, Rui ^{[1
,2
]}

机构：

[1] CHLN Hosp Santa Maria, Serv Med 2, Lisbon, Portugal

[2] Univ Lisbon, Fac Med, Inst Mol Med, P-1699 Lisbon, Portugal

[3] CHLN Hosp Santa Maria, Serv Hematol & Transplantacao Medula, Lisbon, Portugal

[4] CHLN Hosp Santa Maria, Serv Neurol, Lisbon, Portugal

[5] CHLN Hosp Santa Maria, Serv Anat Patol, Lisbon, Portugal

[6] CHLN Hosp Santa Maria, Serv Imagiol Neurol, Lisbon, Portugal

来源：

CLINICAL CASE REPORTS | 2016年 / 4卷 / 04期

关键词：

Brain lymphoma; hemophagocitic lymphohistiocytosis; intravascular lymphoma; white matter abnormalities;

D O I：

10.1002/ccr3.507

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Key Clinical Message Hemophagocytic lymphohistiocytosis (HLH) should be considered in the differential diagnosis of adult patients with white matter disease. Brain involvement can be life-threatening and should prompt aggressive therapy. Even after HLH remission, the possibility of subsequent deterioration due to emergence of an aggressive intravascular lymphoma is highlighted here.

引用

页码：327 / 330

页数：4

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