Journal Article

Juvenile polyposis syndrome might be misdiagnosed as familial adenomatous polyposis: a case report and literature review

Zhao, Zi Ye, Bai, Chen Guang, Zhang, Wei, Xu, Xiao Dong, Du, Yi Qi, Li, Juan, Yan, Hong Li, Gao, Xian Hua, Liu, Lian Jie

2020

Overview

Background Juvenile polyposis syndrome (JPS) is a rare disorder characterized by the presence of multiple juvenile polyps in the gastrointestinal tract, and germline mutations in SMAD4 or BMPR1A. Due to its rarity and complex clinical manifestation, misdiagnosis often occurs in clinical practice. Case presentation A 42-year-old man with multiple pedunculated colorectal polyps and concomitant rectal adenocarcinoma was admitted to our hospital. His mother had died of colon cancer. He was diagnosed with familial adenomatous polyposis (FAP) and underwent total proctocolectomy and ileal pouch anal anastomosis. Two polyps were selected for pathological examination. One polyp had cystically dilated glands with slight dysplasia. The other polyp displayed severe dysplasia and was diagnosed as adenoma. Three years later, his 21-year-old son underwent a colonoscopy that revealed more than 50 pedunculated colorectal juvenile polyps. Both patients harbored a germline pathogenic mutation in BMPR1A . Endoscopic resection of all polyps was attempted but failed. Finally, the son received endoscopic resection of polyps in the rectum and sigmoid colon, and laparoscopic subtotal colectomy. Ten polyps were selected for pathological examination. All were revealed to be typical juvenile polyps, with cystically dilated glands filled with mucus. Thus, the diagnosis of JPS was confirmed in the son. A review of the literatures revealed that patients with JPS can sometimes have adenomatous change. Most polyps in patients with JPS are benign hamartomatous polyps with no dysplasia. A review of 767 colorectal JPS polyps demonstrated that 8.5% of the polyps contained mild to moderate dysplasia, and only 0.3% had severe dysplasia or cancer. It is difficult to differentiate juvenile polyps with dysplasia from adenoma, which could explain why juvenile polyps have been reported to have adenomatous changes in patients with JPS. Therefore, patients with JPS, especially those with concomitant dysplasia and adenocarcinoma, might be easily diagnosed as FAP in clinical practice. Conclusions Juvenile polyp with dysplasia is often diagnosed as adenoma, which might lead to the misdiagnosis of JPS as FAP. The differential diagnosis of JPS versus FAP, should be based on comprehensive evaluation of clinical presentation, endoscopic appearance and genetic investigations; not on the presence or absence of adenoma.

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Adenocarcinoma / Adenoma / Adenomatous Polyposis Coli - diagnosis / Adenomatous Polyposis Coli - genetics / Adult / Analysis / Anastomosis / Bone Morphogenetic Protein Receptors, Type I - genetics / Case Report / Case reports / Colon cancer / Colonoscopy / Colorectal cancer / Colorectal surgery / Comparative analysis / Diagnosis / Diagnostic Errors / Differential diagnosis / Dysplasia / Endoscopy / Familial adenomatous polyposis / Familial polyposis / Family medical history / Gastroenterology / Gastrointestinal tract / Genes / Genetic counseling / Genetic disorders / Genomics / Germ-Line Mutation / Glands / Health education / Hepatology / Histology / Humans / Internal Medicine / Intestinal polyposis / Intestinal Polyposis - congenital / Intestinal Polyposis - diagnosis / Intestinal Polyposis - genetics / Juvenile polyposis syndrome / Laparoscopy / Literature reviews / Male / Medicine / Medicine & Public Health / Misdiagnosis / Mutation / Neoplastic Syndromes, Hereditary - diagnosis / Neoplastic Syndromes, Hereditary - genetics / Patients / Polyps / Proteins / Rectum / Smad4 protein / Smad4 Protein - genetics / Smooth muscle / Tumors / Young Adult