A Peutz–Jeghers syndrome family associated with sinonasal adenocarcinoma: 28 years follow up report

Author:

Chiang Jy-MingORCID,Chen Tse-Ching

Funder

Chang Gung Research Foundation

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics(clinical),Oncology,Genetics

Reference15 articles.

1. Peutz JLA (1921) Over een zeer merkwaardige, gecombineerde familiaire polyposis van de slijmliezen van den tractus intestinalis met die van de neuskeelholte en gepaard met eigenaardige pigmentaties van huid-enslijmvliezen. Ned Maandschr Gen 10:134–146

2. Cerqua N, D’Ottavi LR, Perrotti V et al (1993) Rare manifestation of nasal polyposis in the Peutz–Jeghers syndrome. Acta Otorhinolaryngol Ital 13:333–338

3. De Facq L, De Sutter J, De Man M et al (1995) A case of Peutz–Jeghers syndrome with nasal polyposis, extreme iron deficiency anemia, and hamartoma-adenoma transformation: management by combined surgical and endoscopic approach. Am J Gastroenterol 90:1330–1332

4. Keller JJ, Westerman AM, de Rooij FW, Wilson JH, van Dekken H, Giardiello FM, Weterman MA Offerhaus GJ (2002) molecular genetic evidence of an association between nasal polyposis the Peutz–Jeghers syndrome. Ann Intern Med 136:855–856

5. de Leng WW, Westerman AM, Weterman MA, Keller JJ (2007) Nasal polyposis in Peutz–Jeghers syndrome: a distinct histopathological and molecular genetic entity. J Clin Pathol 60(4):392–396

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