• <em>APC</em> c.4621C&gt;T variant causing Gardner's syndrome in a Han Chinese family may be inherited through maternal mosaicism
• A Case of Long-Term Survival with Tumor Resection and DOX plus DTIC Therapy for Desmoid Tumor after FAP Surgery
• A giant abdominal aggressive fibromatosis resulting in rapid death of a 29-year-old man with familial adenomatous polyposis
• A lesion suspected of being a desmoid tumor in the context of familial adenomatous polyposis should be biopsied
• A novel large deletion in the APC gene associated with Gardner syndrome in a Chinese family
• A paediatric jaw lump: Desmoid tumour
• A successful operation for giant intra-abdominal desmoid tumors associated with familial adenomatous polyposis: A case report
• A Surgical Case of Desmoid Tumor in the Transverse Mesocolon with Pancreatic Invasion
• Accumulated genetic mutations leading to accelerated initiation and progression of colorectal cancer in a patient with Gardner syndrome: A case report
• Adipocyte-rich <em>CTNNB1</em>-mutated Intramuscular Gardner Fibroma Progressing to Desmoid Fibromatosis
• Aggressive mutation in a familial adenomatous polyposis syndrome family: when phenotype guides clinical surveillance
• Approach to screening for Familial Adenomatous Polyposis (FAP) in a cohort of 226 patients with Desmoid-type Fibromatosis (DF): experience of a specialist center in the UK
• Assessment of circulating microRNA specific for patients with familial adenomatous polyposis
• Author's reply: "A lesion suspected of being a desmoid tumor in the context of familial adenomatous polyposis should be biopsied"
• Biology and signaling pathways involved in the oncogenesis of desmoid tumors
• Case report: A rare case of desmoid-type fibromatosis originating in the small intestine
• Chemoprevention in familial adenomatous polyposis: past, present and future
• Clinical application of next-generation sequencing for the management of desmoid tumors: A case report and literature review
• Colectomy and desmoid tumours in familial adenomatous polyposis: a systematic review and meta-analysis
• Correlation Between the Severity of Adhesions and Desmoid Disease in Patients With Familial Adenomatous Polyposis: A Prospective Cohort Study
• CRISPR-SID: Identifying EZH2 as a druggable target for desmoid tumors via in vivo dependency mapping
• Current clinical practice for familial adenomatous polyposis in Japan: A nationwide multicenter study
• Cutaneous desmoid-type fibromatosis: A rare case with molecular profiling
• Deep-penetrating-nevus-like melanoma arising in patients with familial adenomatous polyposis syndrome
• Desmoid Tumor and Multiple Colon Adenomas
• Desmoid Tumors in Familial Adenomatous Polyposis Patients: Favorable Outcomes with Multidisciplinary Management
• Desmoid tumors: Are there still any surgical indications?
• Desmoid tumors: diagnostic and therapeutic considerations
• Desmoid tumour: rare presentation following neonatal lumbar puncture
• Desmoid Tumours of the extremity and trunk. A retrospective study of 44 patients
• Desmoid tumours: a perfect example for making progress in treatment management through international collaboration
• Desmoid type fibromatosis, from radical excision to molecular extirpation
• Desmoid-Type Fibromatosis
• Desmoid-type fibromatosis in children. Clinical features, treatment response, and long-term follow-up
• Diagnostic imaging and CEUS findings in a rare case of Desmoid-type fibromatosis. A case report
• Dispelling misconceptions in the management of familial adenomatous polyposis
• Does ileoanal pouch surgery increase the risk of desmoid in patients with familial adenomatous polyposis?
• Effect of genetic profiling on surgical decisions at hereditary colorectal cancer syndromes
• Evaluation of diagnostic algorithm and therapeutic interventions for intra-abdominal desmoid tumors
• Evolving strategies for management of desmoid tumor
• Expanding the pediatric oncology medical home: Successful utilization of a medical-legal partnership at a pediatric oncology referral center
• Extracolonic cancer risk in Dutch patients with APC (adenomatous polyposis coli)-associated polyposis
• Familial adenomatosis polyposis-related desmoid tumours treated with low-dose chemotherapy: results from an international, multi-institutional, retrospective analysis
• Familial adenomatous polyposis associated with desmoid tumors presenting with abdominal abscess: A case report and literature review
• Familial adenomatous polyposis, desmoid tumors and Gardner syndrome
• Familial adenomatous polyposis: complex patient management
• Fertility preservation and PGT-M in women with familial adenomatous polyposis-associated desmoid tumours
• Gardner Syndrome With Breast Desmoid Tumors
• Gardner syndrome with giant abdominal desmoid tumor during pregnancy: a case report
• Gardner syndrome with maxillofacial manifestation: A case report
• Gardner's syndrome, a rare disease
• Gastric polyposis and desmoid tumours as a new familial adenomatous polyposis clinical variant associated with <em>APC</em> mutation at the extreme 3'-end
• Genotype-phenotype correlation in 99 familial adenomatous polyposis patients: A prospective prevention protocol
• Germline mutations of the adenomatous polyposis coli (APC) gene in Algerian familial adenomatous polyposis cohort: first report
• Giant mesenteric fibromatosis associated with non-Hodgkin lymphoma. A case report and literature review
• High cumulative risk of colorectal cancers and desmoid tumours and fibromatosis in South Asian APC mutation carriers
• Highly aggressive thoracic desmoid tumors in adolescent siblings with fatal outcomes in an FAP kindred: a need for increased vigilance and intervention in at-risk AYAs
• Human microRNA expression in sporadic and FAP-associated desmoid tumors and correlation with beta-catenin mutations
• Ⅰ. Evidence-Based Drug Treatment for Desmoids-Anti-Cancer Drugs, Molecular-Targeted Drugs
• Identification of aggressive Gardner syndrome phenotype associated with a de novo <em>APC</em> variant, c.4666dup
• Immunohistochemical evaluation of potential molecular targets of desmoid-type fibromatosis
• Intra-abdominal desmoid tumors in familial adenomatous polyposis: How much do clinical and surgical variables interfere with their development?
• IPAA Is More "Desmoidogenic" Than Ileorectal Anastomosis in Familial Adenomatous Polyposis
• Large Desmoid Tumor of the Pancreas: A Report of a Rare Case and Review of the Literature
• Life-threatening presentation of complicated intra-abdominal desmoid tumour in a young man without a family history of familial adenomatous polyposis
• Long-term chemoprevention in patients with adenomatous polyposis coli: an observational study
• Long-term clinical outcomes and follow-up status in Japanese patients with familial adenomatous polyposis after radical surgery: a descriptive, retrospective cohort study from a single institute
• Management of ampullary adenomas in familial adenomatous polyposis syndrome: 16 years of experience from a tertiary cancer center
• Management of Desmoid Disease in Familial Adenomatous Polyposis
• Management of familial adenomatous polyposis and MUTYH-associated polyposis; new insights
• Management of serious complications in intra-abdominal desmoid-type fibromatosis
• Medulloblastoma and familial adenomatous polyposis: Good prognosis and good quality of life in the long-term?
• Medulloblastomas associated with an APC germline pathogenic variant share the good prognosis of CTNNB1-mutated medulloblastomas
• Multifocal occurrence of extra-abdominal desmoid type fibromatosis - A rare manifestation. A clinicopathological study of 6 sporadic cases and 1 hereditary case
• Novel intra-genic large deletions of CTNNB1 gene identified in WT desmoid-type fibromatosis
• Novel neoplasms associated with syndromic pediatric medulloblastoma: integrated pathway delineation for personalized therapy
• Novel pathogenic alterations in pediatric and adult desmoid-type fibromatosis - A systematic analysis of 204 cases
• Pancreas sparing duodenectomy in the treatment of primary duodenal neoplasms and other situations with duodenal involvement
• PANCREATIC SOLID-PSEUDOPAPILLARY NEOPLASM IN PATIENTS WITH FAMILIAL ADENOMATOUS POLYPOSIS
• Pediatric peripheral nerve tumors: clinical and surgical aspects
• Percutaneous ultrasound-guided radiofrequency ablation for giant desmoid tumors of the intra-abdominal cavity in a patient with Gardner syndrome
• Periosteal Reaction Possibly Induced by Pazopanib: A Case Report and Literature Review
• Presentation and Follow-up of Familial Adenomatous Polyposis: Differences Between APC and MUTYH Mutations
• Radiation Therapy for Benign Disease: Arteriovenous Malformations, Desmoid Tumor, Dupuytren Contracture, Graves Ophthalmopathy, Gynecomastia, Heterotopic Ossification, Histiocytosis
• Recent trends in the morbidity and mortality in patients with familial adenomatous polyposis: a retrospective single institutional study in Japan
• Ruptured mesenteric desmoid-type fibromatosis without emergency surgery: A rare case report
• Setting the international research agenda for sarcomas with patients and carers: results of phase II of the Sarcoma Patient Advocacy Global Network (SPAGN) priority setting partnership
• Short-term and long-term outcomes after preventive surgery in adolescent patients with familial adenomatous polyposis
• Specimen Identification Errors in Breast Biopsies: Age Matters. Report of Two Near-Miss Events and Review of the Literature
• Superior Mesenteric Artery Pseudoaneurysms in Patients With Familial Adenomatous Polyposis-Associated Intra-abdominal Desmoids: Case Series
• Surgical management of abdominal desmoids: a systematic review and meta-analysis
• The CDK 4/6 inhibitor ribociclib has activity in the treatment of inoperable desmoid tumor. A case report
• The cost-saving effect of centralized histological reviews with soft tissue and visceral sarcomas, GIST, and desmoid tumors: The experiences of the pathologists of the French Sarcoma Group
• The importance of genetics for timing and extent of surgery in inherited colorectal cancer syndromes
• The Role of Pharmacotherapeutic Agents in Children with Desmoid Tumors
• The Role of Radiation Therapy for Symptomatic Desmoid Tumors
• Tumorperforation eines mesenterialen und retroperitonealen Desmoidtumors bei familiärer adenomatöser Polyposis
• Update from the 5th Edition of the World Health Organization Classification of Head and Neck Tumors: Familial Tumor Syndromes
• Web-Based Model for Predicting Time to Surgery in Young Patients with Familial Adenomatous Polyposis: An Internally Validated Study
• β-catenin S45F mutation results in apoptotic resistance