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Eccrine angiomatous hamartoma in a child.儿童的小汗腺血管瘤样错构瘤
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2
Eccrine angiomatous hamartoma: report of five congenital cases.小汗腺血管瘤性错构瘤:5例先天性病例报告。
Pediatr Dermatol. 2009 May-Jun;26(3):316-9. doi: 10.1111/j.1525-1470.2008.00777.x.
3
Successful treatment of eccrine angiomatous hamartoma with botulinum toxin.肉毒杆菌毒素成功治疗小汗腺血管瘤性错构瘤。
Arch Dermatol. 2009 Mar;145(3):241-3. doi: 10.1001/archdermatol.2008.575.
4
Eccrine angiomatous hamartoma associated with spontaneous regression.与自发性消退相关的小汗腺血管瘤性错构瘤
Pediatr Dermatol. 2006 Sep-Oct;23(5):516-7. doi: 10.1111/j.1525-1470.2006.00298.x.
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Eccrine angiomatous hamartoma: a case report and review of the literature.小汗腺血管瘤样错构瘤:一例报告并文献复习
Cutis. 2003 Jun;71(6):449-55.
6
Eccrine angiomatous hamartoma.小汗腺血管瘤样错构瘤
J Am Acad Dermatol. 2002 Sep;47(3):429-35. doi: 10.1067/mjd.2002.121030.
7
Eccrine angiomatous hamartoma: a report of symmetric and painful lesions of the wrists.小汗腺血管瘤性错构瘤:一例双侧手腕部对称性疼痛性皮损的报告
Pediatr Dermatol. 2001 Mar-Apr;18(2):117-9. doi: 10.1046/j.1525-1470.2001.018002117.x.
8
Eccrine angiomatous hamartoma: report of a case and literature review.小汗腺血管瘤样错构瘤:1例报告及文献复习
J Am Acad Dermatol. 1999 Jul;41(1):109-11. doi: 10.1016/s0190-9622(99)70416-0.
9
Eccrine angiomatous hamartoma.小汗腺血管瘤样错构瘤
J Dermatol Surg Oncol. 1994 Dec;20(12):837-8. doi: 10.1111/j.1524-4725.1994.tb03716.x.
10
Eccrine angiomatous hamartoma (nevus): immunohistochemical findings and review of the literature.小汗腺血管瘤性错构瘤(痣):免疫组化结果及文献综述
J Cutan Pathol. 1994 Feb;21(1):71-5. doi: 10.1111/j.1600-0560.1994.tb00694.x.

青春期女孩初潮后出现突然增大并伴有疼痛的小汗腺血管瘤性错构瘤。

Eccrine angiomatous hamartoma with sudden enlargement and pain in an adolescent girl after menarche.

作者信息

Kikusawa Ayuko, Oka Masahiro, Taguchi Kumiko, Shimizu Hideki, Kunisada Makoto, Nishigori Chikako

机构信息

Division of Dermatology; Department of Internal Related; Kobe University Graduate School of Medicine; Kobe, Japan.

出版信息

Dermatoendocrinol. 2011 Oct;3(4):266-8. doi: 10.4161/derm.3.4.15365. Epub 2011 Oct 1.

DOI:10.4161/derm.3.4.15365
PMID:22259656
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3256345/
Abstract

Eccrine angiomatous hamartoma (EAH) is a rare, benign cutaneous lesion characterized histologically by a proliferation of eccrine glands and vascular structures-generally capillaries-in the middle and deep dermis. Sudden enlargement of EAH lesions with or without pain has been noted during puberty and pregnancy and has been attributed to hormonal stimulation. We herein describe a case of EAH that became symptomatic in an adolescent girl. A 13-year-old girl presented with pain associated with a sudden enlargement of a previously asymptomatic swelling on her right second toe. She had an 8-year history of an asymptomatic swelling on her right second toe, and the symptoms appeared approximately 1 year after menarche. Physical examination revealed swelling of the plantar surface of her right second toe. The overlying surface was erythematous with a small amount of fine scales. The biopsied tissue showed a nodular proliferation of eccrine glands intimately admixed with numerous small vessels in the deep dermis and subcutaneous fat tissue. Mucin deposition was present in the stroma surrounding the proliferating eccrine coils and ducts and in the upper dermis. A diagnosis of EAH was made. We suggest that hormonal changes during puberty may have played a role in the rapid growth and pain in the present case.

摘要

小汗腺血管瘤样错构瘤(EAH)是一种罕见的良性皮肤病变,其组织学特征为小汗腺和血管结构(通常为毛细血管)在真皮中层和深层增生。EAH病变在青春期和孕期可出现突然增大,伴或不伴有疼痛,这被认为与激素刺激有关。我们在此报告一例青春期女孩出现症状的EAH病例。一名13岁女孩因右足第二趾先前无症状的肿物突然增大并伴有疼痛前来就诊。她右足第二趾有无症状肿物已有8年病史,症状在初潮后约1年出现。体格检查发现右足第二趾跖面肿胀。肿物表面皮肤发红,有少量细鳞屑。活检组织显示真皮深层和皮下脂肪组织中有小汗腺结节状增生,并与大量小血管紧密混合。增生的汗腺螺旋管和导管周围的间质以及真皮上层有黏液沉积。诊断为EAH。我们认为青春期的激素变化可能在本例的快速生长和疼痛中起了作用。