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考登病患者甲状腺腺瘤样甲状腺肿内发生的乳头状癌。

Papillary carcinoma occurring within an adenomatous goiter of the thyroid gland in Cowden's disease.

作者信息

Kameyama K, Takami H, Miyajima K, Mimura T, Hosoda Y, Ito K, Ito K

机构信息

Division of Diagnostic Pathology, Keio University Hospital, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan.

出版信息

Endocr Pathol. 2001 Spring;12(1):73-6. doi: 10.1385/ep:12:1:73.

DOI:10.1385/ep:12:1:73
PMID:11478271
Abstract

Cowden's disease is an autosomal dominant disorder characterized by multiple benign and malignant neoplastic lesions involving many organs. The presence of characteristic cutaneous lesions is crucial for the diagnosis. Thyroid disease is a major extracutaneous manifestation of this disease; however, the histologic characteristics have not been described in detail. We report a case of thyroid tumor associated with Cowden's disease. Grossly, the tumor showed a multinodular appearance, like an adenomatous goiter. Microscopically, it consisted of follicular adenomas with a trabecular pattern. Some of the nodules had a second component resembling papillary carcinoma. This was thought to be a unique histological feature not described previously, and might be specific to thyroid tumor associated with Cowden's disease.

摘要

考登病是一种常染色体显性疾病,其特征为累及多个器官的多种良性和恶性肿瘤性病变。特征性皮肤病变的存在对诊断至关重要。甲状腺疾病是该疾病的主要皮肤外表现;然而,其组织学特征尚未得到详细描述。我们报告一例与考登病相关的甲状腺肿瘤病例。大体上,肿瘤呈多结节外观,类似腺瘤样甲状腺肿。显微镜下,它由具有小梁状结构的滤泡性腺瘤组成。一些结节有第二个成分,类似乳头状癌。这被认为是一种以前未描述过的独特组织学特征,可能是考登病相关甲状腺肿瘤所特有的。

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Papillary carcinoma occurring within an adenomatous goiter of the thyroid gland in Cowden's disease.考登病患者甲状腺腺瘤样甲状腺肿内发生的乳头状癌。
Endocr Pathol. 2001 Spring;12(1):73-6. doi: 10.1385/ep:12:1:73.
2
Association of multinodular goiter with breast carcinoma: Cowden's disease.多结节性甲状腺肿与乳腺癌的关联:考登病。
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Eur Thyroid J. 2020 Sep;9(5):243-246. doi: 10.1159/000506422. Epub 2020 Mar 12.
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[Hereditary thyroid cancer].[遗传性甲状腺癌]
Chirurg. 2008 Nov;79(11):1017-28. doi: 10.1007/s00104-008-1558-y.
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Abnormal distribution and hyperplasia of thyroid C-cells in PTEN-associated tumor syndromes.PTEN相关肿瘤综合征中甲状腺C细胞的异常分布与增生。

本文引用的文献

1
Cowden Syndrome.考登综合征
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Cowden's disease. A possible new symptom complex with multiple system involvement.考登病。一种可能涉及多系统的新症状复合体。
Ann Intern Med. 1963 Jan;58:136-42. doi: 10.7326/0003-4819-58-1-136.
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Inhibition of cell migration, spreading, and focal adhesions by tumor suppressor PTEN.肿瘤抑制因子PTEN对细胞迁移、铺展和粘着斑的抑制作用。
Endocr Pathol. 2004 Spring;15(1):55-64. doi: 10.1385/ep:15:1:55.
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P-TEN, the tumor suppressor from human chromosome 10q23, is a dual-specificity phosphatase.PTEN是一种来自人类10号染色体长臂23区的肿瘤抑制因子,是一种双特异性磷酸酶。
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Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.考登病(一种遗传性乳腺癌和甲状腺癌综合征)中PTEN基因的种系突变。
Nat Genet. 1997 May;16(1):64-7. doi: 10.1038/ng0597-64.
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Differential loss of heterozygosity in the region of the Cowden locus within 10q22-23 in follicular thyroid adenomas and carcinomas.滤泡性甲状腺腺瘤和癌中位于10q22 - 23的考登基因座区域杂合性的差异丧失。
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Localization of the gene for Cowden disease to chromosome 10q22-23.考登病基因定位于10号染色体q22 - 23区域。
Nat Genet. 1996 May;13(1):114-6. doi: 10.1038/ng0596-114.
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Cowden syndrome (multiple hamartoma syndrome).考登综合征(多发性错构瘤综合征)。
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