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Incidental discovery of a sacral rib: a case report.
Surg Radiol Anat
May 2023
Laboratoire d'anatomie, Université de Picardie Jules Verne, Amiens, France.
Purpose: The observation of an accessory bone joined to the sacrum (suggestive of a sacral rib) prompted us to describe the structure's morphology and its anatomic relationships and to consider its morphogenesis and clinical implications.
Method: A 38-year-old woman underwent computed tomography, to characterize the extension of a thoracic mass. We compared our observations with the literature data.
[Malignant transformation of sacrococcygeal teratoma with voluminous mesentery cyst: a case study conducted in Bamako].
Pan Afr Med J
October 2019
Service de Radiologie, CHU Gabriel Touré, Bamako, Mali.
Malignant sacrococcygeal teratoma is a rare congenital embryonal tumor at high risk of malignant transformation. We report the case of a 20-month old female infant. She was the couple's fourth child.
View Article and Find Full Text PDFLipomyelocele with osseous dysraphic hamartoma in a child: a case report.
J Pediatr Orthop B
July 2010
Section of Radiology, Santa Casa de Misericórdia de São Paulo, Brazil.
Lipomyelocele is a well-known vertebral malformation that affects intraspinal and extraspinal tissues and compartments. However, other tissues can be associated with the lipomatous component, such as well-developed bones in unusual sites. This association is consistent with dysraphic hamartoma, one of the rarest malformations of the vertebral canal closure.
View Article and Find Full Text PDF[A voluminous sacrococcygeal teratoma: prenatal diagnosis, in-utero treatment and obstetric management].
Gynecol Obstet Fertil
October 2007
Clinique gynécologique et obstétricale, CHU Charles-Nicolle, 1, rue de Germont, 76031 Rouen, France.
Sacrococcygeal teratoma is the most common and benign fetal tumor. Fetuses with sacrococcygeal tumors that are predominantly solid and highly vascularized have a high risk of fatal issue. Hydrops and tumor hemorrhage are associated with a highest risk of fetal death.
View Article and Find Full Text PDF[A case of presacral myelolipoma].
Minerva Chir
February 2001
Dipartimento di Oncologia dell'Università, Divisione di Chirurgia Oncologica, Ospedale San Giovanni Battista, Molinette, Corso A. Dogliotti, 14-10126 Torino.
Myelolipoma is a rare benign pathology whose pathogenesis is still unclear. It is most frequently localised in the adrenal gland, followed by the presacral region, mediastinum, and perirenal and hepatic region. It varies in size from a few millimetres to several centimetres.
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