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Fetal Rhabdomyoma of the upper Extremity in a 31-Year Old Patient: a Case Report.
Arch Bone Jt Surg
March 2019
Department of Orthopaedics and Traumatology, Medical University of Graz, Auenbruggerplatz 5, Graz, Austria.
Fetal rhabdomyomas (RM) are extremely rare benign mesenchymal tumours that occur primarily in the head and neck. This tumour exhibits immature skeletal muscle differentiation. The patients' median age is four years and surgical resection is the recommended treatment.
View Article and Find Full Text PDFPrenatal diagnosis of cardiac rhabdomyoma associated with tuberous sclerosis: report of 3 cases.
Neuro Endocrinol Lett
December 2015
Department of Neonatology, Jessenius Medical Faculty in Martin, Comenius University in Bratislava, University Hospital in Martin, Slovakia.
Cardiac rhabdomyoma is the most common cardiac tumor in fetal life, accounting for 60-86% of primary fetal cardiac tumors. It is primarily benign, originating form myocardial muscles and consisting of immature myocytes. About 50-60% of these tumors are associated with tuberous sclerosis.
View Article and Find Full Text PDF[Extracardial rhabdomyoma: a clinicopathologic analysis of 9 cases].
Zhonghua Bing Li Xue Za Zhi
November 2014
Department of Oral Pathology, Ninth People's Hospital, School of Medicine, Shanghai Jiaotong University, E-mail:
Objective: To investigate the clinicopathologic characteristics, differential diagnosis and biological behavior of extracardiac rhabdomyoma.
Methods: Nine cases of extracardiac rhabdomyoma diagnosed between January of 1997 and July of 2014 were reviewed. The clinical, pathologic and immunohistochemical profiles were evaluated.
Foetal rhabdomyoma with fine-needle aspirate cytology correlation.
Singapore Med J
April 2009
Histopathology Department, Singapore General Hospital, Outram Road, Singapore.
A case of intermediate form of foetal rhabdomyoma with cytological correlation is reported in a ten-year-old girl who presented with a lump in the right neck region. Fine-needle aspirate of the lump was performed. Cytological findings were that of spindled cells and rhabdomyoblasts with abundant eosinophilic cytoplasm.
View Article and Find Full Text PDFA 46 XY phenotypic female adolescent with bilateral gonadal tumors consisting of five different components.
Int J Gynecol Pathol
July 2008
Department of Pathology and Laboratory Medicine, University of Rochester Medical Center, Rochester, New York 14642, USA.
46 XY gonadal dysgenesis patients often develop gonadal tumors, including gonadoblastoma and other types of germ cell tumors. We report a case of a 16-year-old female adolescent with primary amenorrhea and a right adnexal mass. Subsequent study revealed that she is a 46 XY phenotypic female adolescent with complete gonadal dysgenesis and with no alterations of the sex-determining region Y gene.
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