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法伯病中的齿状突浸润和脊髓压迫:造血干细胞移植的逆转作用

Odontoid infiltration and spinal compression in Farber Disease: reversal by haematopoietic stem cell transplantation.

作者信息

Jarisch Andrea, Steward Colin G, Sörensen Jan, Porto Luciana, Kieslich Matthias, Klingebiel Thomas, Bader Peter

机构信息

Department of Paediatric Oncology and Haematology, Goethe University Frankfurt, Hospital for Children and Adolescents, Theodor-Stern-Kai 5, 60590, Frankfurt am Main, Germany,

出版信息

Eur J Pediatr. 2014 Oct;173(10):1399-403. doi: 10.1007/s00431-013-2098-0. Epub 2013 Jul 24.

Abstract

Farber disease (FD) is a lysosomal storage disorder caused by accumulation of ceramide in various organs and tissues, most notably the central nervous system, subcutaneous tissues and respiratory tract. We report a girl who developed major destructive bone involvement, which affected the odontoid process and produced spinal compression at 9 years of age. Bone involvement was proven histologically but resolved, as assessed by serial MRI scanning, following matched unrelated donor haematopoietic stem cell transplantation. This transplant resulted in only partial donor chimerism (less than 10 % donor cells in peripheral blood), yet this was sufficient to almost normalize acid ceramidase levels in leukocytes and to produce dramatic improvements in subcutaneous nodules and joint mobility as well as the beneficial effect on the involved bone. Unfortunately, the transplant was rejected after 2 years but the patient was rescued from an aplastic state by successful haploidentical peripheral blood stem cell transplantation and remained a full donor chimera without recurrence of the bone involvement and with steadily improving mobility at the age of 17 years. We describe an FD patient who presented with severe destruction of the odontoid by inflammatory tissue which was reversed after long-term control achieved by allogeneic hematopoietic stem cell transplantation. After extensive literature search, we believe that this is the first report of bony involvement in Farber disease.

摘要

法伯病(FD)是一种溶酶体贮积症,由神经酰胺在各个器官和组织中蓄积所致,最显著的是中枢神经系统、皮下组织和呼吸道。我们报告了一名9岁女童,其出现严重的破坏性骨受累,累及齿状突并导致脊髓受压。组织学证实有骨受累,但在接受匹配无关供者造血干细胞移植后,经系列磁共振成像扫描评估,骨受累情况得到缓解。此次移植仅导致部分供者嵌合(外周血中供者细胞少于10%),但这足以使白细胞中的酸性神经酰胺酶水平几乎恢复正常,并使皮下结节和关节活动度显著改善,以及对受累骨骼产生有益影响。不幸的是,移植在2年后被排斥,但患者通过成功的单倍体相合外周血干细胞移植从再生障碍状态中获救,在17岁时仍为完全供者嵌合体,骨受累未复发且活动度持续改善。我们描述了一名FD患者,其齿状突被炎性组织严重破坏,在通过异基因造血干细胞移植实现长期控制后得以逆转。经过广泛的文献检索,我们认为这是法伯病骨受累的首例报告。

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