Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Chest Wall Hamartoma"'
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 73, Iss, Pp 102009-(2021)
Background chest wall hamartoma is one of the rare findings in the practice of pediatrics surgery. The usual origin of chest wall hamartoma in literature are the ribs. Here we report a very rare case of hamartoma arising from the subcutaneous tissue
Publikováno v:
Open Journal of Radiology. :292-297
Chest wall hamartoma is a very rare tumour with benign course and distinct clinical, radiological, and histopathological characteristics. The lesion develops during foetal life and is present at or shortly after birth. It should be kept in differenti
Autor:
Ricardo K. Kalil
Publikováno v:
Tumors and Tumor-Like Lesions of Bone ISBN: 9781447165774
Tumors and Tumor-Like Lesions of Bone ISBN: 9783030283148
Tumors and Tumor-Like Lesions of Bone ISBN: 9783030283148
Chest wall hamartoma is a congenital malformation of bone composed of mature cartilage sometimes with foci of enchondral ossification, a loose connective tissue containing reactive bone spicules, and aneurysmal bone cyst-like areas, arising in the ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55a2aa89c7b0dacbb02b9abc91541638
https://doi.org/10.1007/978-1-4471-6578-1_76
https://doi.org/10.1007/978-1-4471-6578-1_76
Publikováno v:
Pediatric Endosurgery & Innovative Techniques. 8:267-271
Introduction: Thoracoscopic-assisted resection of thoracic aneurysmal bone cyst has never been described in the literature. Infantile cartilaginous hamartoma of the rib is a large tumor characterized by cartilaginous, vascular, and mesenchymal elemen
Publikováno v:
Journal of Pediatric Surgery. 36:1346-1349
Mesenchymal hamartomas of the chest wall are rare benign lesions usually discovered in infancy. The authors present their experience with 3 cases. All of these cases were managed initially conservatively, although 1 child required a thoracotomy and p
Publikováno v:
Pediatric Surgery International. 22:398-400
Mesenchymal hamartoma of the chest wall is an unusual lesion remarkable for its occurrence in early infancy and alarming clinical presentation, which often suggests malignancy. Despite its aggressive appearance and propensity to attain massive size,
Publikováno v:
Ultrasound in Obstetrics and Gynecology. 7:453-455
We present the prenatal evaluation and diagnosis of a disorganized chest wall hamartoma (with underlying sternal cleft in a family with a prior offspring with the VATER association. The possibility that these conditions are linked to mesodermal defec
Publikováno v:
Journal of Clinical Ultrasound. 24:83-85
Publikováno v:
Fetal diagnosis and therapy. 9(4)
A fetal chest wall hamartoma successfully treated by surgical resection after birth is described. Ultrasonography showing a heterogeneous partially calcified thoracic tumor allowed in utero diagnosis.
Publikováno v:
Pediatric pathology. 14(1)
We present one case of a chest wall hamartoma diagnosed in a 4-week-old boy. This entity is an extremely rare but characteristic congenital malformation of the ribs in infancy. To avoid maltreatment, it has to be distinguished from benign and maligna