Abnormalities in C-type lectin-like receptor 2 in a patient with Gorham-Stout disease: the first case report

被引:2
|
作者
Oishi, Saori [1 ]
Tsukiji, Nagaharu [1 ]
Segawa, Takahiro [2 ]
Takano, Katsuhiro [1 ]
Hasuda, Norio [3 ]
Suzuki-Inoue, Katsue [1 ,4 ]
机构
[1] Univ Yamanashi, Fac Med, Dept Clin & Lab Med, Yamanashi, Japan
[2] Univ Yamanashi, Ctr Life Sci Res, Yamanashi, Japan
[3] Univ Yamanashi, Dept Surg, Yamanashi, Japan
[4] Univ Yamanashi, Fac Med, Dept Clin & Lab Med, 1110 Shimokato,Chuo, Yamanashi 4093898, Japan
关键词
CLEC-2; Gorham-Stout disease; lymphangiomatosis; lymphatic vessels; platelets; PLATELET ACTIVATION; CLEC-2; FEATURES; SYK;
D O I
10.1016/j.rpth.2023.102273
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Gorham-Stout disease (GSD) is a form of lymphangiomatosis of unknown etiology, characterized by abnormal distribution of lymphatic vessels. Platelets and lymphangiogenesis are closely related via C-type lectin-like receptor 2 (CLEC-2)/podoplanin.Key Clinical Question: Despite similarities between abnormal lymphatic vessels in CLEC-2-deficient mice and patients with GSD, whether CLEC-2 on platelets is involved in GSD pathogenesis is unknown.Clinical Approach: We examined CLEC-2 expression in platelets of a patient with lethal GSD. Most of the patient's platelets expressed aberrant CLEC-2 that was not detectable by certain monoclonal antibodies for human CLEC-2. Further, this population was not activated by a CLEC-2-activating snake venom, rhodocytin. Possible causes of abnormal CLEC-2 including anti-CLEC-2 autoantibodies, podoplanin binding to CLEC-2, and pathogenic CLEC1B gene alteration were excluded.Conclusions: We believe that this is the first report of a patient with structurally and functionally abnormal CLEC-2. CLEC-2 abnormality may be associated with dysregulated lymphangiogenesis in GSD.
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页数:5
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