Literature DB >> 26347965

Management of Tumors of the Ischiorectal Fossa: The Role of Percutaneous Biopsy.

Nicolas C Buchs1, Neil J Mortensen, Richard J Guy, Max Gibbons, Bruce D George.   

Abstract

BACKGROUND: Noninflammatory masses in the ischiorectal fossa are rare.
OBJECTIVE: This study aimed to review our experience with ischiorectal fossa tumors and to address the question of whether percutaneous biopsy should be undertaken.
DESIGN: This is a retrospective study. SETTINGS: This study was conducted at a tertiary institution. PATIENTS: From April 2007 to November 2014, all consecutive ischiorectal fossa masses treated in a referral center were retrospectively reviewed. They were all presented and discussed in a multidisciplinary team meeting. Magnetic resonance imaging was performed in all the patients. Inflammatory pathologies, such as abscess, were excluded from the analysis.
INTERVENTIONS: Percutaneous biopsy and surgical excision of ischiorectal fossa tumors were reviewed. MAIN OUTCOME MEASURES: Perioperative, pathological, and oncological outcomes were measured.
RESULTS: Eleven patients were identified (8 female; median age, 50 years; range, 25-90). Percutaneous biopsy was undertaken in 8 patients. All biopsies were diagnostic and altered preoperative management in 3 cases (aggressive angiomyxoma (n = 2), desmoid fibromatosis (n = 1)). Overall final diagnosis was benign in 3 patients, locally aggressive neoplasm in 3, and malignant in 5 cases (leiomyosarcomas (n = 2), liposarcomas (n = 2), and angiomyosarcoma (n = 1)). Surgical approaches were perineal in 8 patients, abdominoperineal in 1 patient, and totally abdominal in 1 patient. One patient (age 90 years) was managed nonsurgically. After resection, 2 positive margins were observed (R1 rate, 20%). After a mean follow-up of 24.3 months, 3 patients have experienced local recurrence, which required further surgery in 2 cases. LIMITATIONS: This study is limited by the small number of patients.
CONCLUSIONS: Noninflammatory masses in the ischiorectal fossa are rare, but they are commonly malignant and should be imaged by MRI. Unless the radiological appearances are diagnostic, percutaneous biopsy is recommended and alters management in about one-third of cases.

Entities:  

Mesh:

Year:  2015        PMID: 26347965     DOI: 10.1097/DCR.0000000000000438

Source DB:  PubMed          Journal:  Dis Colon Rectum        ISSN: 0012-3706            Impact factor:   4.585


  4 in total

1.  Aggressive angiomyxoma presenting as an ischiorectal fossa tumour.

Authors:  Ma Corazon Concepcion Cabanilla-Manuntag; Marc Paul Jose Lopez; Mayou Martin Tampo; Czar Louie Gaston
Journal:  BMJ Case Rep       Date:  2020-04-28

2.  Ischiorectal fossa metastasis from colon cancer: Case report of a rare entity and review of literature.

Authors:  Areej Mohammed Alzamil; Abdullah Saleh AlQattan; Ahmed Abdulmajeed Alanazi; Turki Alshammari; Mohammed Tahtouh
Journal:  Int J Surg Case Rep       Date:  2021-04-27

3.  Pelvic Lipoblastoma with Extension into Ischiorectal Fossa and Abdominal Lipoblastoma - Complete Excision by Laparoscopy in Children - A Report of Two Cases.

Authors:  Anilkumar Pura Lingegowda; Ramachandra Chandrayya
Journal:  J Indian Assoc Pediatr Surg       Date:  2022-01-11

4.  A rare solitary fibrous tumor in the ischiorectal fossa: a case report.

Authors:  Kazuhiko Morikawa; Shinsuke Takenaga; Koichi Masuda; Asami Kano; Takao Igarashi; Hiroya Ojiri; Kaoru Ueda; Mamoru Ishiyama; Nei Fukasawa
Journal:  Surg Case Rep       Date:  2018-10-03
  4 in total

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