A case of Spitz nevus on the perianal area of a child

2014 ◽  
Vol 70 (5) ◽  
pp. AB34
Keyword(s):  
2015 ◽  
Vol 27 (6) ◽  
pp. 787
Author(s):  
Dong Yeup Lee ◽  
Jong Heon Baek ◽  
Dong Joo Kim ◽  
Soo Kyung Lee ◽  
Myoung Shin Kim ◽  
...  

2020 ◽  
Vol 99 (9) ◽  

Introduction: Perianal hidradenitis suppurativa is a chronic recurrent inflammatory, suppurative, and fistulising disease of apocrine glands, adjacent anal canal and soft tissues. Perianal area is the second most common affected area after axilla. There are three grades of the disease. Hidradenitis suppurativa represents a chronic, recurrent, deep-seated folliculitis resulting in abscesses, followed by the formation of sinus tracts and subsequent scarring. Perianal hidradenitis suppurativa is the last and the most serious grade of the disease and a specific access is needed for patient preparation and surgical treatment alone. The currently preferred method of treatment for patients with extensive perianal hidradentitis is excision and closure with combination of skin flaps, primary suture and skin graft in one or two stages. Case reports: There are three case reports of perianal hidradenitis suppurativa in this article. The local and overall initial treatment of patients followed by a radical excision and closure with a rotation skin flaps and skin grafts is described. The final results were satisfactory, with no recurrence or serious complication.


2015 ◽  
Vol 77 (5) ◽  
pp. 483-486
Author(s):  
Honoka IHARA ◽  
Monji KOGA ◽  
Ryoko TATSUKAWA ◽  
Kaori KOGA ◽  
Yoshitugu SHIBAYAMA ◽  
...  

1998 ◽  
Vol 18 (1) ◽  
pp. 115-123
Author(s):  
Nicholas Smith ◽  
Margaret Evans ◽  
Andrew Pearce ◽  
W. Hamish ◽  
B. Wallace
Keyword(s):  

Author(s):  
Ander Timoteo Delgado ◽  
Laia Falgueras Verdaguer ◽  
Anna Pigem Rodeja ◽  
Ramon Farres Coll

2020 ◽  
Vol 13 (11) ◽  
pp. e236896
Author(s):  
Matthew Pizzuto ◽  
Sarah Ellul ◽  
Mohamed Shoukry

A 14-year-old boy, a known case of perinatal hypoxic cerebral palsy, presented to paediatric emergency with acute melaena and blood staining around feeding gastrostomy site. Physical examination revealed pallor, but no signs of distress with an unremarkable abdominal examination. Routine blood tests revealed normochromic. Abdominal ultrasound scan and Meckel’s scan were unremarkable. The patient underwent examination under anaesthesia of the perianal area and joint upper and lower gastrointestinal endoscopy. Streak-like gastritis with no signs of active bleeding lesions were noted and patchy areas of colitis involving the descending and sigmoid colon and the rectum. All clinical findings and evidence-based diagnosis matched gastric antral vascular ectasia. He was successfully managed conservatively with elemental hydrolysed feeding formula.


2021 ◽  
pp. 176-183
Author(s):  
Thanachat Rutnumnoi ◽  
Charussri Leeyaphan

Extramammary Paget’s disease (EMPD) is a rare intraepithelial neoplasm that occurs in apocrine-bearing areas of skin. Most EMPD patients initially present with chronic pruritic eczematous lesions involving genitalia, perineum and perianal area. Familial form of EMPD is extremely rare. Several genetic mutations have been proposed but specific modes of inheritance are still unknown. This article reports two cases of familial extramammary Paget’s disease in female siblings.


2002 ◽  
Vol 9 (4) ◽  
pp. 209-221 ◽  
Author(s):  
Wolter J. Mooi
Keyword(s):  

2002 ◽  
Vol 10 (1) ◽  
pp. 69-73 ◽  
Author(s):  
B. Clarke ◽  
A. Essa ◽  
R. Chetty
Keyword(s):  

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