[Intraspinal enterogenous cyst. Case report].

Arq Neuropsiquiatr

Faculdade de Medicina de Marília (FAMEMA), SP, Brasil.

Published: June 1997

The authors report the case of a 7 years old boy with cervical pain and tetraparesis progressing by two months. He presented an intraspinal cystic lesion from C4 to C6. Exeresis of the lesion was undergone by anterior way through a corpectomy of C5-C6 followed by reconstruction with bone graft of the iliac crest and metallic plaque. Anatomic diagnosis of the lesion was enterogenous cyst. Aspects of clinical presentation, embryology and treatment of these cysts are discussed.

Download full-text PDF

Source
http://dx.doi.org/10.1590/s0004-282x1997000200023DOI Listing

Publication Analysis

Top Keywords

enterogenous cyst
8
[intraspinal enterogenous
4
cyst case
4
case report]
4
report] authors
4
authors report
4
report case
4
case years
4
years boy
4
boy cervical
4

Similar Publications

Enterogenous cysts (ECs) are rare, benign, congenital ectopic endodermal cysts that only occasionally involve the central nervous system. We presented the diagnosis and treatment of an exceedingly rare case of EC located in the brainstem, which has previously been reported only seven times in pediatric patients. The patient underwent complete surgical resection and experienced no recurrence during the 6-month follow-up.

View Article and Find Full Text PDF

Intraspinal enterogenous cysts are rare congenital abnormalities that mainly develop in the spinal canal, more commonly in the cervical and thoracic regions, and rarely in the lumbar spine. We present a case of neurenteric (NE) cyst in the conus medullaris and cauda equina junction at the level of L1 in a patient presenting with a nine-year history of progressive lower limb weakness, paresthesia, and muscle wasting. The patient underwent complete resection of the cyst and had no postoperative complications with marked improvement of paresthesia and some localized pain in the lower back manageable by analgesics.

View Article and Find Full Text PDF

Background: Bronchogenic cysts are rare developmental anomalies that belong to the category of congenital enterogenous cysts. They arise from lung buds and are present at birth. The embryonic foregut is their origin.

View Article and Find Full Text PDF

Mesenteric cysts are mostly congenital cysts of varied etiology. They occur twice as often in females than in males. They have varied clinical presentations.

View Article and Find Full Text PDF

Ethnopharmacological Relevance: The Niaodukang mixture (NDK) is a preparation known for its ability to lower serum creatine levels in individuals with chronic kidney disease (CKD) and is commonly administered at medical facilities like the Zhongshan Hospital of Traditional Chinese Medicine. The initial use of NDK was mainly to treat CKD. Our hospital frequently utilizes NDK, which consists of Rheum officinaleBaill.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!