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角化棘皮瘤:它是一种真实存在的实体吗?

Keratoacanthoma: is it a real entity?

作者信息

Manstein C H, Frauenhoffer C J, Besden J E

机构信息

Division of Plastic Surgery, St. Mary Medical Center, Langhorne, PA, USA.

出版信息

Ann Plast Surg. 1998 May;40(5):469-72. doi: 10.1097/00000637-199805000-00004.

DOI:10.1097/00000637-199805000-00004
PMID:9600429
Abstract

Keratoacanthoma of the skin and well-differentiated squamous cell carcinoma are two cutaneous neoplasms that most often occur in sun-exposed sites of light-skinned persons. It is often difficult to distinguish these two from each other either clinically or histologically. The view that these two cutaneous neoplasms are part of the same disease entity is not new. We reviewed 150 patients with these two diseases in an effort to see whether any specific criteria for diagnosis and treatment could be achieved. It is our hypothesis that they are not separate diseases but within the spectrum of the same disease. Keratoacanthoma may be some sort of aborted malignancy or hyperplastic premalignant lesion within the squamous cell carcinoma spectrum. The incidence of metastases from squamous cell carcinoma of the skin may be as high as 3%. We do not have the courage to wait 3 months to see if a potentially invasive and metastatic neoplasm is indeed involutional. Incision biopsy may be wrought with significant histopathological inconsistencies. We believe that early, complete excision is the treatment of choice for all skin neoplasms thought to be keratoacanthoma.

摘要

皮肤角化棘皮瘤和高分化鳞状细胞癌是两种最常发生在浅肤色人群阳光暴露部位的皮肤肿瘤。无论是在临床上还是组织学上,这两者常常难以区分。这两种皮肤肿瘤属于同一疾病实体的观点并不新鲜。我们回顾了150例患有这两种疾病的患者,试图确定是否能得出任何诊断和治疗的具体标准。我们的假设是,它们并非独立的疾病,而是同一疾病范围内的不同表现。角化棘皮瘤可能是某种鳞状细胞癌谱系内的恶性肿瘤未遂或增生性癌前病变。皮肤鳞状细胞癌的转移发生率可能高达3%。我们没有勇气等待3个月来观察一个潜在的侵袭性和转移性肿瘤是否真的会自行消退。切开活检可能会出现显著的组织病理学不一致情况。我们认为,对于所有被认为是角化棘皮瘤的皮肤肿瘤,早期完整切除是首选的治疗方法。

相似文献

1
Keratoacanthoma: is it a real entity?角化棘皮瘤:它是一种真实存在的实体吗?
Ann Plast Surg. 1998 May;40(5):469-72. doi: 10.1097/00000637-199805000-00004.
2
Diagnostic problem of keratoacanthoma.角化棘皮瘤的诊断问题
Lancet. 1969 Mar 8;1(7593):490-2. doi: 10.1016/s0140-6736(69)91590-6.
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Malignant potential of keratoacanthoma.角化棘皮瘤的恶性潜能。
Laryngoscope. 1979 Jul;89(7 Pt 1):1092-8.
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Invasive squamous cell carcinoma initially diagnosed as a giant keratoacanthoma.最初被诊断为巨大角化棘皮瘤的浸润性鳞状细胞癌。
J Am Acad Dermatol. 1984 Feb;10(2 Pt 2):372-8. doi: 10.1016/s0190-9622(84)80010-9.
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Keratoacanthoma or squamous cell carcinoma? A surgeon's dilemma.
Plast Reconstr Surg. 1966 Jul;38(1):56-62. doi: 10.1097/00006534-196607000-00012.
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[Keratoacanthoma? Better to say "squamous cell carcinoma, keratoacanthoma type"].[角化棘皮瘤?更确切地说是“角化棘皮瘤型鳞状细胞癌”]
Ann Dermatol Venereol. 2008 Aug-Sep;135(8-9):541-6. doi: 10.1016/j.annder.2008.03.001.
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Solitary keratoacanthoma in a child.儿童孤立性角化棘皮瘤
Am J Dis Child. 1974 Jul;128(1):110-11. doi: 10.1001/archpedi.1974.02110260112023.
8
Histopathological diagnosis of epithelial crateriform tumors: Keratoacanthoma and other epithelial crateriform tumors.上皮性火山口状肿瘤的组织病理学诊断:角化棘皮瘤及其他上皮性火山口状肿瘤。
J Dermatol. 2016 Nov;43(11):1321-1331. doi: 10.1111/1346-8138.13390. Epub 2016 Apr 14.
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Subungual keratoacanthoma: a variant of verrucous squamous cell carcinoma of the skin.
Appl Pathol. 1983 Nov-Dec;1(6):339-42.
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[Spinocellular epithelioma and keratoacanthoma. Anatomicoclinical inconsistencies].[棘细胞上皮瘤与角化棘皮瘤。解剖临床方面的不一致性]
Rev Stomatol Chir Maxillofac. 1986;87(5):282-6.

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