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多发性皮脂腺肿瘤伴结肠息肉病和骨骼异常。

Multiple sebaceous gland tumours associated with polyposis of the colon and bony abnormalities.

作者信息

Lynne-Davies G, Brown J

出版信息

Can Med Assoc J. 1974 Jun 22;110(12):1377-9.

PMID:4545832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1947634/
Abstract

The cases are presented of two siblings with multiple cutaneous tumours associated with adenomatous polyps of the colon and bony abnormalities. In one patient an adenocarcinoma of the colon supervened, and there was a history of adenocarcinoma of the colon without the presence of other abnormalities in a third sibling. Clinically the sebaceous tumours resembled sebaceous hyperplasia, but histologically they exhibited features of sebaceous adenoma.The association of a variety of multiple soft tissue tumours, particularly epidermal cysts, with polyposis of the colon and bony abnormalities is well recognized. However, multiple solid sebaceous tumours have not been reported previously as a feature of this syndrome. They should in future alert the physician to the possible presence of multiple polyposis of the colon in affected individuals and immediate relatives.

摘要

本文报告了两例患有多种皮肤肿瘤的兄弟姐妹,这些肿瘤与结肠腺瘤性息肉及骨骼异常相关。其中一名患者后来发生了结肠癌,第三名兄弟姐妹有结肠癌病史,但无其他异常。临床上,皮脂腺肿瘤类似皮脂腺增生,但组织学上表现为皮脂腺瘤的特征。多种软组织肿瘤,特别是表皮囊肿,与结肠息肉病及骨骼异常的关联已得到充分认识。然而,此前尚未有报道称多发性实性皮脂腺肿瘤是该综合征的特征。未来,它们应提醒医生注意受影响个体及其直系亲属可能存在结肠多发性息肉病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/1947634/8d7625cb0a88/canmedaj01584-0058-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/1947634/32c3e602f741/canmedaj01584-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/1947634/fbd299fe073a/canmedaj01584-0058-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/1947634/a7d2db30454f/canmedaj01584-0058-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/1947634/8d7625cb0a88/canmedaj01584-0058-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/1947634/32c3e602f741/canmedaj01584-0058-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/1947634/fbd299fe073a/canmedaj01584-0058-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/1947634/a7d2db30454f/canmedaj01584-0058-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/95b6/1947634/8d7625cb0a88/canmedaj01584-0058-d.jpg

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本文引用的文献

1
Hereditary pattern for multiple osteomas in a family group.一个家族群体中多发性骨瘤的遗传模式。
Am J Hum Genet. 1952 Mar;4(1):31-6.
2
A genetic and clinical study of intestinal polyposis, a predisposing factor for carcinoma of the colon and rectum.一项关于肠道息肉病的遗传学与临床研究,肠道息肉病是结肠癌和直肠癌的一个诱发因素。
Am J Hum Genet. 1951 Jun;3(2):167-76.
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GARDNER'S SYNDROME. A FAMILY GROUP STUDY AND REVIEW.加德纳综合征。一项家族群体研究与综述。
Arch Dermatol. 1964 Jul;90:20-30. doi: 10.1001/archderm.1964.01600010026007.
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Follow-up study of a family group exhibiting dominant inheritance for a syndrome including intestinal polyps, osteomas, fibromas and epidermal cysts.对一个表现出综合征显性遗传的家族群体进行的随访研究,该综合征包括肠息肉、骨瘤、纤维瘤和表皮囊肿。
Am J Hum Genet. 1962 Dec;14(4):376-90.
5
The association of familial polyposis of the colon with multiple sebaceous cysts.结肠家族性息肉病与多发性皮脂腺囊肿的关联。
Br J Surg. 1954 Mar;41(169):534-41. doi: 10.1002/bjs.18004116917.