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Management of intergluteal pilonidal disease

Authors
Daniel J Sullivan, MD, MPH
David C Brooks, MD
Elizabeth Breen, MD
Section Editors
Russell S Berman, MD
Martin Weiser, MD
Deputy Editor
Wenliang Chen, MD, PhD

INTRODUCTION

Intergluteal pilonidal disease is an infection of the skin and subcutaneous tissue at or near the upper part of the natal cleft of the buttocks (figure 1) [1]. Management is variable and guided by the clinical presentation and extensiveness of disease [1-4]. The clinical manifestations and diagnosis are reviewed separately. (See "Intergluteal pilonidal disease: Clinical manifestations and diagnosis".)

ACUTE ABSCESS

An acute pilonidal abscess is managed with an incision and drainage (I&D) procedure at the time of presentation, usually under local anesthesia. This management approach is consistent with that described for a skin and subcutaneous abscess at other sites. (See "Skin abscesses, furuncles, and carbuncles", section on 'Incision and drainage'.)

The incision is generally performed lateral to the midline or over the area of maximal fluctuance, and all visible hair within the sinus is debrided [1,3-5]. Wounds are packed with gauze, and healing occurs by secondary intention in the acute setting. The wound edges may also be marsupialized (oversewing them while incorporating the base of the wound) to prevent premature closure of the skin. Curettage of the pilonidal sinus and tract at time of I&D or excision of midline pores is not typically performed in the clinical setting of an acute infection [4]. The approach to an I&D procedure is described separately. (See "Technique of incision and drainage for skin abscess".)

An I&D, however, is not the definitive procedure for pilonidal disease, as recurrence rates range from approximately 20 to 55 percent [4,6]. In a retrospective review of 73 consecutive patients with a first episode of acute pilonidal abscess treated by I&D, 42 (58 percent) healed primarily, with a median time to healing of five weeks; 9 of the 42 developed recurrence of pilonidal disease at a median follow-up of 60 months [6]. The overall cure rate following I&D was 45 percent.

CHRONIC OR RECURRENT DISEASE

The definitive treatment of chronic or persistent pilonidal disease is a surgical excision of all sinus tracts [1]. The surgical procedures range from simple excision with or without primary closure to complex flap reconstruction.

          

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Literature review current through: Nov 2016. | This topic last updated: Tue Jun 21 00:00:00 GMT+00:00 2016.
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