scholarly journals Intramedullary abscess complicating congenital dermal sinus tract in an infant: A rare occurrence

2017 ◽  
Vol 46 (1) ◽  
pp. 77
Author(s):  
Joseph J Valamparampil ◽  
Ajay Kumar ◽  
Alice Deepa ◽  
Prameela Joji ◽  
S Shajehan
Neurosurgery ◽  
2007 ◽  
Vol 61 (3) ◽  
pp. E661-E661 ◽  
Author(s):  
William J. Mack ◽  
Saadi Ghatan

Abstract OBJECTIVE Congenital dermal sinus tracts most frequently occur in the midline and are often associated with dermoid or epidermoid inclusion cysts. A lateral cranial origin is extremely rare and anatomically inconsistent with an etiology involving closure of the rostral neural tube during embryogenesis. CLINICAL PRESENTATION We describe the first case of a pterional cranial dermal sinus tract associated with a small epidermoid, with extension to the dura of the anterior cranial fossa. INTERVENTION The extra- and intracranial portions of the tract were visualized and resected with the use of an operating microscope. Pathological diagnosis confirmed dermal sinus tract. CONCLUSION We review the existing literature and address the developmental and clinical features pertinent to the management of cranial dermal sinus tracts, emphasizing the need for exploration of these potentially harmful lesions.


2014 ◽  
Vol 29 (10) ◽  
pp. 1277-1282 ◽  
Author(s):  
Mesut Mete ◽  
Ahmet Sukru Umur ◽  
Yusuf Kurtuluş Duransoy ◽  
Mustafa Barutçuoğlu ◽  
Nurcan Umur ◽  
...  

2020 ◽  
Vol 7 ◽  
pp. 2333794X2095332
Author(s):  
Pezad Doctor ◽  
Jocelyn Ang ◽  
Basim Asmar ◽  
Eric McGrath

2008 ◽  
Vol 43 (6) ◽  
pp. 1200-1202 ◽  
Author(s):  
Ifeoma Ikwueke ◽  
Samantha Bandara ◽  
Steven J. Fishman ◽  
Sara O. Vargas

2015 ◽  
Vol 50 (6) ◽  
pp. 339-343 ◽  
Author(s):  
Georgios Papaevangelou ◽  
Parmenion P. Tsitsopoulos ◽  
Nikolaos Flaris ◽  
Charalampos Iliadis ◽  
Christos Tsonidis

2011 ◽  
Vol 51 (6) ◽  
pp. 460-462 ◽  
Author(s):  
Satoshi YAMAGUCHI ◽  
Masaaki TAKEDA ◽  
Hirotaka KIHARA ◽  
Kuniki EGUCHI ◽  
Takafumi MITSUHARA ◽  
...  

1970 ◽  
Vol 33 (1) ◽  
pp. 103-105 ◽  
Author(s):  
Charles R. Neblett ◽  
Pedro C. Caram ◽  
Richard Morris

2021 ◽  
Vol 6 (10) ◽  

Intramedullary spinal abscesses are extremely rare. Most occur secondary to cardiopulmonary spread;contiguous origin is less frequent. Few intramedullary spinal abscesses have been reported secondary to dermal sinus tracts. A dermoid sinus is a congenital lesion (closed simple dysraphism) with rare incidence.Dermoid sinuses can ease local invasion and spinal infections (meningitis, intradural extramedullary and intramedullary abscesses), usually with thoracolumbar involvement. Here we describe acase of a 20-month-old boy who presented with fever and refusal to walk 2 days prior to admission. On examination of the lumbar spine, a small sinus with skin stigmata was noted.Neurological evaluation revealed paraparesis more prominent on the left side, reduced tone and reflexes, left leg hypoesthesia,reduced anal tone, and urinary retention.MRI scan demonstrated intramedullary abscess extending from L2 to S1 level. The patient was urgently admitted for drainage of intramedullary abscess and excision of the dermal sinus tract. Proper antibiotic treatment was completed for 6 weeks with gradual improvement and ultimately full ambulation ability.


2003 ◽  
Vol 15 (1) ◽  
pp. 1-3 ◽  
Author(s):  
Niyazi Nefi Kara

The congenital dermal sinus is an abnormal epithelium-lined sinus tract between the skin surface and deeper tissues. It occurs during neurulation when the neural groove closes to form the neural tube on Day 26 of gestation and results from a failure of neuroectoderm to separate from the cutaneous ectoderm. The most frequent location is the lumbosacral area; an upper thoracic location is quite rare. This 37-year-old man presented with headache and numbness in both arms. No specific neurological findings were observed. Physical examination revealed a dimple at T-2. Radiography and magnetic resonance imaging of the thoracic spine revealed spina bifida at T1–3, a meningocele, and a dermal sinus tract complex. The treatment approach and outcome in this unusual case are presented.


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