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Phospholipase Cδ-4 (PLCδ4) Acts as a Nuclear Player to Influence Cyclin B Expression in the Embryonal Rhabdomyosarcoma Cell Lines RD and A204. [PDF]

Biomolecules
Salucci S, Bavelloni A, Versari I, Burattini S, Bavelloni F, Gobbi P, Fanzani A, Codenotti S, Blalock W, Scotlandi K, Faenza I.   +10 more
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Embryonal rhabdomyosarcoma

International Journal of Oral and Maxillofacial Surgery, 1988
Rhabdomyosarcoma is one of the most common malignancies of the mesenchymal tissue in the head and neck region. A case of a 26-year-old male with oral rhabdomyosarcoma is presented. The clinical and pathologic aspects of this malignancy are also reviewed.
E M, Sadeghi, D J, Gingrass, E J, Surwillo, T, Anderson, T T, Tang   +4 more
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Auricular Embryonal Rhabdomyosarcoma

Dermatology, 1994
Rhabdomyosarcoma is an uncommon tumour that may present at a wide variety of different sites. We report a 4-year-old girl who developed an embryonal rhabdomyosarcoma arising in the left pinna which was clinically indistinguishable from a lymphangioma. The case illustrates that this neoplasm can be easily misdiagnosed because of its variable morphology.
N P, Burrows, R C, Ratnavel, J W, Grant, G C, Cormack, R J, Pye   +4 more
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Vaginal embryonal rhabdomyosarcoma

Voprosy ginekologii, akušerstva i perinatologii, 2021
Vaginal embryonal rhabdomyosarcoma is a relatively rare tumor, which is more commonly diagnosed in children under three years of age and is rarely associated with organ-sparing treatment. Neoadjuvant chemotherapy followed by radiotherapy or surgery can be currently used as local tumor control.
N.I. Minashkina, V.A. Strykov, T.G. Dyadik, I.V. Karachentsova   +3 more
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Embryonal rhabdomyosarcoma

Indian Journal of Otolaryngology, 1987
A rare case of Embryonal Rhabdomyosarcoma of the middle ear and mastoid with distant metastasis in liver and spinal cord is presented.
A. S. Khurana, G. S. Bawa, Jagdeepak Singh   +2 more
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Embryonal rhabdomyosarcoma: Immunohistochemical characterization

Oral Surgery, Oral Medicine, Oral Pathology, 1985
A 15-year-old boy was referred to the ear, nose, and throat clinic because of a swelling in the upper premolar region. The initial diagnosis of a poorly differentiated soft-tissue sarcoma was made. Further immunohistochemical studies established a definitive diagnosis of embryonal rhabdomyosarcoma. The tumor cells coexpressed both desmin, the component
S, Geiger, B, Czernobilsky, G, Marshak, B, Geiger   +3 more
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Embryonal rhabdomyosarcoma of spermatic cord

Urology, 1980
This article discusses 2 patients with embryonal rhabdomyosarcoma of the spermatic cord and presents a survey of the literature and therapeutic methods. In recent years the prognosis of this malignant tumor has improved significantly by virtue of a combination of radical inguinal orchiectomy and retroperitoneal lymph node dissection with supplementary ...
HOEKSTRA, HJ, WOBBES, T, BROUWERS, TM, POSTMA, A, KOOPS, HS   +4 more
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Decoding the ‘embryonic’ nature of embryonal rhabdomyosarcoma

Journal of Developmental Origins of Health and Disease, 2015
Embryonal rhabdomyosarcoma is one of the major defined histologic variants of rhabdomyosarcoma that is mainly reported in children. The histologic appearance of this neoplastic entity recapitulates normal myogenesis. The tumor cells variably exhibit the different cellular phases of myogenesis ranging from undifferentiated mesenchymal cells to elongated
R. Lav, R. Heera, L. M. Cherian
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Auricular embryonal rhabdomyosarcoma

World Journal of Pediatrics, 2022
Javier Arredondo Montero, Mónica Bronte Anaut, Sara Hernández-Martín, Juan Carlos López-Gutiérrez   +3 more
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Embryonal Rhabdomyosarcoma Passed Per Urethra

The Journal of Urology, 2002
Embryonal rhabdomyosarcoma of the prostate is a rare mesenchymal tumor. We describe a 3-year-old boy who passed this lesion per urethra, enhancing the speed to diagnosis and treatment. To our knowledge this is the first reported case of this nature. CASE REPORT A 3-year-old boy presented to the accident and emergency department with difficulty voiding.
M J A, Perry, D J P, Cahill, P L, Denham, H G A, Naerger   +3 more
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