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Management of Tumors of the Ischiorectal Fossa: The Role of Percutaneous Biopsy.
Buchs, Nicolas C; Mortensen, Neil J; Guy, Richard J; Gibbons, Max; George, Bruce D.
Affiliation
  • Buchs NC; 1 Department of Colorectal Surgery, Churchill Hospital, University Hospitals of Oxford, Oxford, United Kingdom 2 Department of Orthopedic Surgery, Nuffield Orthopedic Center, University Hospitals of Oxford, Oxford, United Kingdom.
Dis Colon Rectum ; 58(10): 938-42, 2015 Oct.
Article in En | MEDLINE | ID: mdl-26347965
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.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pelvic Neoplasms / Biopsy / Fibromatosis, Aggressive / Myxoma / Neoplasm Recurrence, Local Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Dis Colon Rectum Year: 2015 Document type: Article Affiliation country: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pelvic Neoplasms / Biopsy / Fibromatosis, Aggressive / Myxoma / Neoplasm Recurrence, Local Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Female / Humans / Male / Middle aged Country/Region as subject: Europa Language: En Journal: Dis Colon Rectum Year: 2015 Document type: Article Affiliation country: Reino Unido