Procedures for Managing Pilonidal Cyst/Abscess

Author(s):  
Wesley D. Davis ◽  
Theresa M. Campo
Keyword(s):  
1970 ◽  
Vol 101 (4) ◽  
pp. 496-496 ◽  
Author(s):  
W. B. Reed
Keyword(s):  

Author(s):  
V.V. Ezhova

The case of prenatal ultrasound diagnosis of pilonidal cyst at 25 weeks of gestation is presented. The diagnosis was confirmed after birth.


2021 ◽  
Vol 108 (Supplement_2) ◽  
Author(s):  
S Kalaskar ◽  
J Adamek

Abstract Introduction The accepted treatment of pilonidal disease still consists of surgical excision with primary wound closure. This treatment has complications such as excessive pain, delayed wound healing, and recurrence. We introduced this technique using a radial laser probe (SiLaCTM, Biolitec, Germany). Previous studies have shown encouraging results with respect to safety, patient satisfaction, and minimal recurrence rates. Method The pilot project was planned with the objectives to assess postoperative complications and reoperation rates. All operations were performed as day case procedures under general anaesthesia. We studied the data of our first 25patients operated with this technique between January 2019 and December 2019 using a prospective database and outpatient clinic follow up. Results The median follow up duration was 13 months. The initial success rate was 64%(16/25), reoperation was required in 32%(8/25) and one patient was lost to follow up. one patient returned with abscess formation in the postoperative period. Conclusions SiLaC is a safe and minimally invasive technique for the destruction of the pilonidal cyst and sinus. The success rate is modest, making this new therapy a minimally invasive option for the majority of the patients with pilonidal disease but it should be offered with caution.


1943 ◽  
Vol 60 (2) ◽  
pp. 264-266 ◽  
Author(s):  
David Brezin ◽  
Carruthers Love ◽  
Joseph Lawrence
Keyword(s):  

2013 ◽  
Vol 2013 ◽  
pp. 1-2
Author(s):  
Luigi Cormio ◽  
Francesca Sanguedolce ◽  
Paolo Massenio ◽  
Giuseppe Di Fino ◽  
Giuseppe Carrieri

Pilonidal sinus is a long-standing chronic inflammatory condition consisting of a sinus tract from the skin-lined orifice extending into subcutaneous tissue, with hairs attached to the wall of the tract and projecting outside of the opening. Penile location is rare, and differential diagnosis with severe balanoposthitis, epidermal cysts, and neoplasms can be difficult. We report a rare case of pilonidal cyst located between coronal sulcus and prepuce which, due to its ulcerated aspect and absence of a tract with projecting hairs, simulated a penile carcinoma.


1997 ◽  
Vol 84 (6) ◽  
pp. 784-784 ◽  
Author(s):  
R. D. Ferdinand ◽  
D. J. Scott ◽  
N. R. McLean
Keyword(s):  

PEDIATRICS ◽  
1965 ◽  
Vol 36 (2) ◽  
pp. 293-293
Author(s):  
ANTHONY SHAW

I take issue with Dr. Lewin's article, Pilonidal Cyst in Infancy, Pediatrics, 35:795, on several counts. First of all and most important, the evidence on which he claims to be making a historical first case report is very shaky indeed. I do not believe that "strongly suggestive" clinical and anatomic evidence is a sufficiently strong platform on which one should base such a claim. Dr. Lewin is basing his entire thesis on the fact that his patient developed an abscess (subsequently a sloughing cellulitis) in an area where congenital sinuses are occasionally observed.


1979 ◽  
Vol 51 (3) ◽  
pp. 383-391 ◽  
Author(s):  
Robert A. Morantz ◽  
John J. Kepes ◽  
Solomon Batnitzky ◽  
Byron J. Masterson

✓ Spinal ependymomas may rarely arise from heterotopic ependymal cell clusters and thus occur in an extraspinal location. Presentation of three cases and a review of the literature reveal that these tumors have characteristic radiographic and clinical features. They occur mainly in patients in the third decade of life, and present either in the soft tissue posterior to the sacrum or in the pelvis. In the case of posterior tumors, the patient exhibits a mass which is usually mistaken for a pilonidal cyst. Patients whose tumor is pelvic in location present with sphincter disturbances or dysfunction of the sacral nerve roots. Conventional and computerized tomographic studies will reveal erosion of the sacrum. Myelography will demonstrate an extradural mass indenting the thecal sac from below. The protein in the cerebrospinal fluid will be normal. A combined posterior and anterior approach with the goal of complete tumor removal is the procedure of choice. If this is not feasible, then radiation therapy should be employed. Because of the increased incidence of systemic metastases, the average postoperative survival is approximately 10 years.


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