Histopathological hallmarks of cutaneous lesions of capillary malformation-arteriovenous malformation syndrome

被引:15
作者
Valdivielso-Ramos, M. [1 ]
Torrelo, A. [2 ]
Martin-Santiago, A. [3 ]
Hernandez-Nunez, A. [4 ]
Azana, J. M. [5 ]
Campos, M. [6 ]
Berenguer, B. [7 ]
Garnacho, G. [8 ]
Moreno, R. [9 ]
Colmenero, I [10 ]
机构
[1] Hosp Infanta Leonor, Dermatol Dept, Madrid, Spain
[2] Hosp Nino Jesus, Dermatol Dept, Madrid, Spain
[3] Hosp Son Espases, Dermatol Dept, Mallorca, Spain
[4] Hosp Fuenlabrada, Dermatol Dept, Madrid, Spain
[5] Hosp Albacete, Dermatol Dept, Albacete, Spain
[6] Hosp Gregorio Maranon, Dermatol Dept, Madrid, Spain
[7] Hosp Gregorio Maranon, Plast Surg Dept, Madrid, Spain
[8] Hosp Reina Sofia, Dermatol Dept, Cordoba, Spain
[9] Hosp Henares, Dermatol Dept, Madrid, Spain
[10] Hosp Nino Jesus, Pathol Dept, Madrid, Spain
关键词
VASCULAR ANOMALIES; SOMATIC MUTATION; WEBER-SYNDROME; RASA1; CLASSIFICATION; EXPRESSION;
D O I
10.1111/jdv.16326
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Importance Capillary malformation-arteriovenous malformation (CM-AVM) syndrome is a recently described syndrome with distinctive cutaneous lesions. Very little is known about the histopathology of these lesions. Objective The purpose of the study was to evaluate the histopathological characteristics of the pink macules of the CM-AVM syndrome and to investigate if these pink macules could be classified as capillary malformations or arteriovenous malformations based on their histopathological features. Design-settings-participants We conducted a retrospective multicenter study involving eight hospitals in Spain. Fifteen biopsies from pink macules of the CM-AVM syndrome were analysed and compared with five biopsies of diverse capillary malformations and three stage I arteriovenous malformations. Results Pink macules' biopsies of the CM-AVM syndrome showed similar features including a high vascular density encompassing capillaries and numerous thick-walled arterioles mainly located in the superficial dermis, a predominance of elongated over round vessels, scarce or absent erythrocytes within the lumina and discrete perivascular inflammation. CMs were characterized by an increased number of capillary-type vessels mostly rounded and located in the upper dermis. AVMs were composed by highly increased numbers of vessels with a branching pattern involving the full thickness of the dermis, without erythrocytes within the lumina. Wilms tumour 1 protein was positive in the endothelial cells both in pink macules of the CM-AVM and in arteriovenous malformations. Conclusions and relevance Pink macules of the CM-AVM syndrome seem to be different from capillary malformations. Our results suggest that histologically and immunohistochemically they are closer to incipient arteriovenous malformations than to capillary malformations. A deepened knowledge about the nature of these skin lesions will contribute to the better understanding of capillary malformation-arteriovenous malformation syndrome, and will open the possibility of new and more specific treatments in the future.
引用
收藏
页码:2428 / 2435
页数:8
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