Retinal Involvement in a Patient with Cerebral Manifestation of Chronic Graft-Versus-Host-Disease

被引:4
作者
Blecha, Christiane [1 ]
Angstwurm, Klemens [2 ]
Wolff, Daniel [3 ]
Holler, Ernst [3 ]
Helbig, Horst [1 ]
Grassinger, Jochen [3 ]
Rennert, Janine [4 ]
Kleiter, Ingo [5 ]
Huber, Elisabeth [6 ]
Schmid, Christoph [7 ]
Dietrich-Ntoukas, Tina [1 ,8 ]
机构
[1] Univ Med Ctr Regensburg, Dept Ophthalmol, D-93053 Regensburg, Germany
[2] Univ Med Ctr Regensburg, Dept Neurol, D-93053 Regensburg, Germany
[3] Univ Med Ctr Regensburg, Dept Internal Med 3, D-93053 Regensburg, Germany
[4] Univ Med Ctr Regensburg, Inst Radiol, D-93053 Regensburg, Germany
[5] Ruhr Univ Bochum, St Josef Hosp, Dept Neurol, Bochum, Germany
[6] Univ Med Ctr Regensburg, Dept Pathol, D-93053 Regensburg, Germany
[7] Klinikum Augsburg, Dept Internal Med 2, Augsburg, Germany
[8] Charite Univ Med Berlin, Dept Ophthalmol, Berlin, Germany
关键词
Chronic graft-versus-host-disease; Hematology; STEM-CELL TRANSPLANTATION; CONSENSUS CONFERENCE; CLINICAL-PRACTICE; CHRONIC GVHD;
D O I
10.1159/000439490
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: We report a 35-year-old female patient with cerebral manifestations of chronic graft-versus-host disease (cGvHD) and putative retinal involvement after allogeneic peripheral blood stem cell transplantation (alloHSCT). Patient and Methods: The patient experienced recurrent episodes of fever and encephalitic signs 7 months after alloHSCT during taper of immunosuppression (IS). Results: Cerebral magnetic resonance imaging (MRI) showed non-gadolinium-enhancing confluent periventricular lesions and cerebrospinal fluid inflammation. After exclusion of infectious causes, treatment with steroids and antiepileptics improved cognitive deficits. Steroid reduction provoked a relapse responding to IS. 2 years later, she complained of right-sided blurred vision and floaters; both eyes showed whitish circumscribed retinal infiltrations, cellular infiltration of the vitreous and mild bilateral optic disc edema. Oncological and neurological work-up ruled out infectious diseases and other GvHD manifestations. Symptoms and signs resolved under continued systemic IS, leaving pigmented retinal scars. After IS withdrawal, classical cutaneous cGvHD developed, resolving on systemic IS. 94 months after transplantation, she is doing well. Conclusion: To our knowledge, this is the first observation of retinal involvement of cerebral cGvHD manifestations with retinal infiltrations documented in the absence of other causes and in parallel to periventricular lesions in cerebral MRI. Based on bone marrow histology, we discuss a small vessel pathophysiology of cGvHD. (C) 2015 S. Karger GmbH, Freiburg
引用
收藏
页码:532 / 534
页数:3
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