ganglioneuroma/وذمة

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مقالاتالتجارب السريريةبراءات الاختراع

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11 النتائج

Thoracic ganglioneuromas resulting in nonimmune hydrops fetalis.

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Introduction Most often, ganglioneuromas affect older pediatric and adult patients. They are typically slow growing tumors that remain clinically silent until they become large enough to cause symptoms by compression of adjacent structures. Case We report a case of a 22-year-old Hispanic gravida 2

Multiple mediastinal ganglioneuromas: report of a case.

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A 23-year-old male known to have an asymptomatic mediastinal mass for four years was admitted due to progressive pitting edema of his arms and legs lasting for one week. The edema subsided prior to surgical extirpation of the left paraspinal mass. Initially recognized radiologically as a

Laparoscopic resection of primary adrenal ganglioneuroma: A case report and review of the literature.

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Adrenal ganglioneuroma (AGN) is an extremely rare, benign tumor that originates from the neural crest tissue of the sympathetic nervous system. The majority of cases are detected incidentally, since the disease often lacks clear clinical manifestations or is asymptomatic. In addition, AGN is often

[A case of gangliocytoma: a six-year follow-up of cyst formation].

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We report a case of gangliocytoma at a cortical and subcortical area in the right parietal lobe. The patient had a generalized seizure at 11 years of age. The MRI shows an ill-demarcated high intensity area in T2 weighted images including an enhancing tumor of 10 mm in diameter. At first, the tumor

The pathogenesis of cysts accompanying intra-axial primary and metastatic tumors of the central nervous system.

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Recent reports have suggested that cyst formation accompanying astrocytomas in the central nervous system (CNS) is due to an edematous process caused by blood-brain barrier (BBB) disruption and not a result of necrosis. This study is performed to investigate whether the hypothesis of cyst formation

Prenatal ultrasonographic diagnosis of fetal intracranial tumors: a review.

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Our objective was to review current literature pertaining to prenatal ultrasonography of various fetal intracranial neoplastic and non-neoplastic tumors. To this goal, all manuscripts published in the English language regarding this topic obtained from a MEDLINE search from 1966 through January 1998

Utility of neurophysiological monitoring using dorsal column mapping in intramedullary spinal cord surgery.

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OBJECTIVE Intramedullary spinal cord tumors can displace the surrounding neural tissue, causing enlargement and distortion of the normal cord anatomy. Resection requires a midline myelotomy to avoid injury to the posterior columns. Locating the midline for myelotomy is often difficult because of the

[The ultrasonic antenatal diagnosis of rarely encountered tumors in fetuses and the procedure for managing the pregnancy and labor].

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Ultrasonic examinations of 3000 pregnant women revealed congenital developmental defects in 22 (0.7%) fetuses: in 4 cases tumors of various sites were detected and in 2 cases the tumors were found in one of the twins. Pathologic and histologic examinations carried out after delivery revealed a

[Neuroradiological findings of relatively rare tumors of the brain].

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In the publication by the World Health Organization of the histological classification of central nervous system tumors in 1993, several new tumor types were added, including pleomorphic xanthoastrocytoma (PXA), dysembryo-plastic neuroepithelial tumor (DNT), and desmoplastic infantile ganglioglioma

Compound adrenal medullary tumor.

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Compound tumors of the adrenal medulla, characterized by a mixture of pheochromocytoma and ganglioneuroma, are rare, only 12 cases having been reported in the literature. We present the case of a 66-year-old woman with a left-sided incidentally discovered adrenal mass that was subsequently shown to

From the archives of the AFIP: superficial gliomas: radiologic-pathologic correlation. Armed Forces Institute of Pathology.

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Glial neoplasms that are peripherally located and involve the cortical gray matter are noteworthy because of their predilection to serve as a seizure locus, their amenability to surgical resection, their generally favorable prognosis, and their characteristic imaging features, which facilitate

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