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Groen RJ, van Ouwerkerk WJ. Cerebellar dermoid tumor and occipital meningocele in a monozygotic twin: clues to the embryogenesis of craniospinal dysraphism. Childs Nerv Syst. 1995 Jul; 11(7): 414-7.

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Article

Occipital Dermal Sinus Tract Causing Craniospinal Infection: Case Report and Review of Literature

1Neurosurgical Resident, Montreal Neurological Institute and Hospital - McGill University, Montreal, Canada

2Department of Neurosurgery, Khoula Hospital, Muscat, Oman

3Department Radiology, Khoula Hospital, Muscat, Oman


American Journal of Medical Case Reports. 2018, Vol. 6 No. 5, 81-86
DOI: 10.12691/ajmcr-6-5-2
Copyright © 2018 Science and Education Publishing

Cite this paper:
Tariq Al-Saadi, Ahmed Al Habsi, Zahra Al Hajri. Occipital Dermal Sinus Tract Causing Craniospinal Infection: Case Report and Review of Literature. American Journal of Medical Case Reports. 2018; 6(5):81-86. doi: 10.12691/ajmcr-6-5-2.

Correspondence to: Tariq  Al-Saadi, Neurosurgical Resident, Montreal Neurological Institute and Hospital - McGill University, Montreal, Canada. Email: t.dhiyab@hotmail.com

Abstract

Background: Congenital dermal sinus tract (DST) is a rare entity of cranial or spinal dysraphism that may occur anywhere from nasion and along the midline neuraxis from occipital to sacral regions. Craniospinal infection caused by occipital DST is even rarer. Because of their scarcity, these lesions are not well documented in the literature, often mixed with dermal sinuses in other location or other dysmorphic features. This paper reports a unique case of an infant presented with craniospinal abscesses resulting from occipital dermal sinus tract. Methods and materials: In this paper, we report a case of a 16-month-old girl presented with high grade fever, vomiting and lethargy. She had a discharging occipital skin lesion. Her diagnosis was "Occipital DST with Cerebellospinal Abscess", which was treated successfully by excision of the DST and cerebellar abscess. Histopathological examination revealed a dermoid cyst. She received 8 weeks of parenteral antibiotic treatment with a good outcome. Results: Occipital DST is a rare condition. Its clinical presentation varies and clinical suspicion is required. Early neurosurgical intervention is important to prevent the risk of potential complications such as abscess and bacterial meningitis. Conclusion: This case highlights the importance of early recognition and evaluation of midline craniospinal cutaneous stigmata in infant. Further neurosurgical assessment with radiological investigations are recommended for early detection and management. Once diagnosed is made, surgical intervention and appropriate antibiotic therapy are the mainstay of treatment.

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