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Indocyanine green fluorescence imaging-assisted laparoscopy resection of retroperitoneal tumors in children: case report and literature review.
Front Pediatr
June 2024
Department of Gastrointestinal Surgery, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, China.
This study examined the applicability of indocyanine green (ICG) fluorescence imaging to assist the laparoscopic resection of retroperitoneal tumors in pediatric patients via an abdominal approach. Conducted prospectively at the Guangzhou Women and Children's Medical Center from May to September 2023, the research included three pediatric cases, for whom laparoscopic retroperitoneal tumor resections were performed utilizing ICG fluorescence imaging. In each case, ICG was intravenously administered (0.
View Article and Find Full Text PDFGanglioneuroblastoma arising in a Mature Cystic Teratoma of Ovary: Report and Literature review of an uncommon neoplasm.
Gynecol Oncol Rep
December 2022
AdventHealth - Central Florida Division South, Orlando, FL, United States.
•Somatic neoplasms in Mature Cystic Teratoma are uncommon; Ganglioneuroblastoma is rare, this is 2nd reported case.•Due to rarity, it can pose a diagnostic challenge for Pathologists, and management and staging conundrum for Gynecologists.•Morphological differentials include immature teratoma, glial neoplasms arising in teratoma, and carcinoid.
View Article and Find Full Text PDFSuprasellar central nervous system ganglioneuroblastoma: a case in a 9-year-old child and review of the literature.
Childs Nerv Syst
November 2020
Department of Neurosurgery, Pennsylvania State University College of Medicine, Hershey, PA, 17033, USA.
Purpose: Intracranial ganglioneuroblastomas are incredibly rare neuroectodermal tumors with only 8 described cases total, 5 of those having imaging findings METHODS: Here we present a 9-year-old female patient with 4 months progressive headaches, personality changes, and vomiting. We also present a review of the current literature of intracranial ganglioneuroblastomas.
Results: Imaging demonstrated a partially calcified suprasellar mass measuring 4.
Surgical strategy for an adult patient with a catecholamine-producing ganglioneuroblastoma and a cerebral aneurysm: a case report.
Surg Case Rep
September 2018
Department of Surgery, Graduate School of Medicine, Tohoku University, 1-1 Seiryou-machi, Aobaku, Sendai, 980-8574, Japan.
Background: Ganglioneuroblastomas, particularly those that produce catecholamine, are extremely rare in adults. Here, we report an interesting surgical case of an adult patient with a catecholamine-producing ganglioneuroblastomas in her adrenal gland, suspected to be a pheochromocytoma, and with a cerebral aneurysm.
Case Presentation: The patient was a 73-year-old woman under treatment for hypertension.
Ganglioneuroblastoma Arising in an Ovarian Dermoid Cyst: First Report in the Literature.
Int J Gynecol Pathol
January 2019
Department of Pathology, Belfast Health and Social Care Trust, Belfast, Northern Ireland, United Kingdom (S.R., W.G.M.) Douglass Hanly Moir Pathology, Sydney, New South Wales, Australia (D.J.).
The development of a somatic neoplasm within an ovarian dermoid cyst (mature cystic teratoma) is a rare, but well described, phenomenon which occurs in approximately 1% of all cases. Any of the tissue components of a dermoid cyst has the potential to undergo neoplastic transformation with carcinoid tumors and squamous cell carcinomas being among the most common neoplasms. We report a case of a ganglioneuroblastoma arising within an ovarian dermoid cyst, an association which, as far as we are aware, has not been described previously.
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