- Cowden Disease Associated with Lhermitte-Duclos Disease: A Case Report
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Park BR, Kim EJ, Choi WS
- KMID: 2024445
- J Korean Radiol Soc.
- 2006 Oct;55(4):327-331.
- doi: 10.3348/jkrs.2006.55.4.327
Cowden's disease (CD) is rare multiple hamartoma-neoplasia syndrome. Lhermitte-Duclos disease (LDD) is well known to be a hamartoma of the cerebellum. CD may be accompanied with LDD and other multiple... -
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- Breast Cancer in Cowden Syndrome: A Case Report
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Jung MH
- KMID: 1471191
- J Korean Soc Radiol.
- 2009 Apr;60(4):279-282.
- doi: 10.3348/jksr.2009.60.4.279
Cowden syndrome is rare condition with characteristic multiple hamartoma and mucocutaneous lesions. It is important for radiologists to be aware of Cowden syndrome because the patients with this disease have... -
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- Fibrous hamartoma of infancy manifested as multiple nodules: a case report
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Jung PM, Hong EK
- KMID: 1421507
- J Korean Med Sci.
- 1990 Dec;5(4):243-247.
- doi: 10.3346/jkms.1990.5.4.243
Fibrous hamartoma of infancy is an uncommon benign fibrous proliferation, usually presenting as a solitary nodule. A rare example of multiple fibrous hamartoma of infancy is described. Two masses which... -
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- Autosomal Dominant Inherited Cowden's Disease in a Family
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Ha JW
- KMID: 1792646
- Clin Endosc.
- 2013 Jan;46(1):85-90.
- doi: 10.5946/ce.2013.46.1.85
Cowden's disease, also known as a kind of phosphatase and tensin homolog (PTEN) hamartoma tumor syndrome, is an uncommon autosomal dominant inherited complex disorder with various hamartomatous growths of multiple... -
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- Lhermitte-Duclos Disease Associated with Cowden Disease
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Choi ES, Rhee BA, Koh JS, Kim TS
- KMID: 1904532
- J Korean Neurosurg Soc.
- 2003 Oct;34(4):375-378.
Lhermitte-Duclos disease, or dysplastic gangliocytoma of the cerebellum, is a peculiar hamartoma arising from the cerebellar cortex. Cowden disease, which is also termed as a multiple hamartoma-neoplasia syndrome, is an... -
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- A Case of Cowden Syndrome Associated with Breast Cancer and Thyroid Cancer
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Hong EJ, Kim HK, Cho YS, Ji JS, Kim CW, Kim CW, Lee BI, Chae HS, Han SW, Choi KY
- KMID: 2244069
- Korean J Gastrointest Endosc.
- 2006 Apr;32(4):293-297.
Cowden syndrome, which is also known as 'multiple hamartoma syndrome', is an autosomal dominant condition with variable expression resulting from a mutation in the PTEN gene on the chromosome arm,... -
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- A Case of Cowden Syndrome
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Hong WK, Song HJ, Lee HS, Lee JR, Shin JH, Choi GS
- KMID: 2302170
- Korean J Dermatol.
- 2007 Aug;45(8):829-831.
Cowden syndrome is a rare autosomal dominant disorder characterized by mucocutaneous alterations including multiple facial trichilemmomas, oral mucosal papillomatosis, and acral keratoses. Extracutaneous lesions include polyposis of the gastrointestinal tract,... -
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- A case of Cowden's syndrome associated with Lhermitte-Duclos disease
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Lim DK, Kim SE, Song JY, Kim DH, Kim SJ, Park MI, Park SJ
- KMID: 2081650
- Korean J Med.
- 2009 Apr;76(Suppl 1):S31-S34.
Cowden's disease, or multiple hamartoma syndrome, is an uncommon autosomal dominant condition characterized by mucocutaneous lesions and systemic malignancies. Lhermitte-Duclos disease, or dysplastic gangliocytoma of the cerebellum, is a rare... -
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- Cowden Disease: Case Report and Review of the Literature
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Son JH, Chung BY, Jung MJ, Choi YW, Kim HO, Park CW
- KMID: 2444866
- Ann Dermatol.
- 2019 Jun;31(3):325-330.
- doi: 10.5021/ad.2019.31.3.325
Cowden's disease is a rare autosomal dominant, multiple hamartoma syndrome with characteristic mucocutaneous lesions. It is associated with abnormalities of the breast, thyroid, and gastrointestinal tract; and is characterized by... -
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- Cowden Syndrome with a Novel Germline PTEN Mutation and an Unusual Clinical Course
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Seol JE, Park IH, Lee W, Kim H, Seo JK, Oh SH
- KMID: 2352502
- Ann Dermatol.
- 2015 Jun;27(3):306-309.
- doi: 10.5021/ad.2015.27.3.306
Here, we report a case of Cowden syndrome with an unusual clinical course of late-onset oral papillomatosis and a novel germline PTEN mutation. Cowden syndrome is the most common phosphatase... -
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- Two Cases of Sclerotic Fibroma
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Yoon CH, Ro YS
- KMID: 2302769
- Korean J Dermatol.
- 2004 Nov;42(11):1466-1469.
Sclerotic fibroma is an uncommom fibrotic neoplasm that can occur as solitary lesions in otherwise healthy individuals. Multiple sclerotic fibromas of the skin are considered a cutaneous marker of multiple... -
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- Cowden's disease--a report on the first case in Korea and literature review
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Lee HR, Moon YS, Yeom CH, Kim KW, Chun JY, Kim HK, Choi HS, Kim DK, Chung TS
- KMID: 645122
- J Korean Med Sci.
- 1997 Dec;12(6):570-575.
- doi: 10.3346/jkms.1997.12.6.570
Cowden's disease, or multiple hamartoma syndrome, is an uncommon condition with characteristic mucocutaneous lesions associated with abnormalities of the breast, thyroid, and gastrointestinal tract. We describe a 32-year-old man... -
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- Cowden Syndrome Detected by FDG PET/CT in an Endometrial Cancer Patient
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Kang YH, Lee HK, Park G
- KMID: 2351650
- Nucl Med Mol Imaging.
- 2016 Sep;50(3):255-257.
- doi: 10.1007/s13139-016-0427-8
Cowden syndrome (CS) is a rare autosomal dominant disorder characterized by multiple hamartomas in various tissues and cancers (breast, thyroid, and endometrium). We report CS of the esophagus and gastrointestinal... -
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- Bannayan-Riley-Ruvalcaba Syndrome in a Patient with a PTEN Mutation Identified by Chromosomal Microarray Analysis: A Case Report
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Lee SH, Ryoo E, Tchah H
- KMID: 2375281
- Pediatr Gastroenterol Hepatol Nutr.
- 2017 Mar;20(1):65-70.
- doi: 10.5223/pghn.2017.20.1.65
Bannayan-Riley-Ruvalcaba syndrome (BRRS) is one of the phosphatase and tensin homolog hamartoma tumor syndrome with a PTEN gene mutation. It is a rare dominant autosomal disorder characterized by cutaneous lipomas,... -
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- PTEN Mutation Identified in Patient Diagnosed with Simultaneous Multiple Cancers
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Won HS, Chang ED, Na SJ, Whang IY, Lee DS, You SH, Kim YS, Kim JS
- KMID: 2437630
- Cancer Res Treat.
- 2019 Jan;51(1):402-407.
- doi: 10.4143/crt.2017.579
PTEN hamartoma tumor syndrome is a spectrum of disorders characterized by unique phenotypic features including multiple hamartomas caused by mutations of the tumor suppressor gene PTEN. Cowden syndrome and Bannayan–Riley–Ruvalcaba... -
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- Multiorgan Involvements of Cowden Disease in a 50-Year-Old Woman: A Case Report and Literature Overview
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Lee EJ, Jung WS, Ko JM, Park HJ
- KMID: 2208809
- J Korean Soc Radiol.
- 2013 Sep;69(3):251-255.
- doi: 10.3348/jksr.2013.69.3.251
Cowden disease is the prototype of phosphate and, tensin homologue deleted on the chromosome 10 (PTEN) hamartoma tumor syndrome caused by germline mutations in the tumor suppressor PTEN, which is... -
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- A Case of Multiple Eyelid Trichilemmoma Associated with Cowden Syndrome
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Cho CH, Son JH
- KMID: 2217050
- J Korean Ophthalmol Soc.
- 2013 May;54(5):803-807.
- doi: 10.3341/jkos.2013.54.5.803
PURPOSE: To report a case of multiple eyelid trichilemmomas associated with Cowden syndrome. CASE SUMMARY: A 27-year-old woman presented with multiple upper and lower eyelid skin masses that developed over several... -
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- Cowden Syndrome Accompanied by Multiple Sclerotic Fibroma on the Face
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Kim ST, Kang DY, Kang JS, Baek JW, Jeon YS, Suh KS
- KMID: 2247643
- Korean J Dermatol.
- 2010 Dec;48(12):1136-1139.
Cowden syndrome (CS) is a rare genodermatosis that is characterized by multiple hamartomatous tumors of an ectodermal, mesodermal and endodermal origin. CS is associated with an increased risk of malignancy... -
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- A Case of Cowden Syndrome Associated with Tumor of the Follicular Infundibulum
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Na CH, Kim YS, Shin B, Kim M
- KMID: 2353439
- Korean J Dermatol.
- 2016 Sep;54(8):650-652.
Cowden Syndrome (CS) is a rare genodermatosis of autosomal-dominant inheritance, with variable expressivity and multiple types of hamartomas. The most consistent features of CS are small wart-like papillomatous papules on... -
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- Synchronous Bilateral Breast Carcinoma in a Patient with Cowden Syndrome with PTEN Mutation: A Case Report
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Kwon SY, Yeo SH, Ha JS, Kang SH
- KMID: 2434908
- J Breast Dis.
- 2018 Dec;6(2):79-83.
- doi: 10.14449/jbd.2018.6.2.79
Cowden syndrome (CS), also known as multiple hamartomas syndrome, is a rare hereditary autosomal dominant disorder caused by a germline mutation in the phosphatase and tensin homolog (PTEN) gene mapped... -
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