8910/3 Embryonal rhabdomyosarcoma, pleomorphic



Definitions

Vulva
ICD-O-3 topography code: C51
ICD10: C51
           

Rhabdomyosarcomas are the most frequent malignant soft tissue tumours in children and adolescents, with embryonal rhabdomyosarcoma as the most common subtype. Typical sites of involvement are the head and neck region and the genitourinary system. Phenotypically and biologically, embryonal rhabdomyosarcomas recapitulate features of embryonal skeletal muscle. Genetically, most cases show loss of chromosomal region 11p15 1
 
Alberto S. Pappo (Ed.)
Pediatric Bone and Soft Tissue Sarcomas
1st Edition
Springer Verlag: Berlin Heidelberg New York 2005



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Three histological variants of embryonal rhabdomyosarcoma have been identified
2
 
Fletcher CDM, Unni KK, Mertens F (Eds.)
World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone.
3rd Edition
IARC Press: Lyon 2002



:

Spindle cell rhabdomyosarcoma
Botryoid rhabdomyosarcoma
Anaplastic rhabdomyosarcoma

Vulvar embryonal rhabdomyosarcomas are found almost exclusively in girls <10 years of age. The tumours typically arise from the labial or perineal area and form solid masses. Patients present with bleeding and ulceration. The prognosis depends on the clinical stage and the histological pattern. An alveolar histology is associated with a poor prognosis, whereas the survival rate for classic embryonal rhabdomyosarcoma is >90%
3
Click to access Pubmed
Copeland LJ, Gershenson DM, Saul PB, Sneige N, Stringer CA, Edwards CL (1985)
Sarcoma botryoides of the female genital tract.
Obstet Gynecol 66: 262-6



4
Click to access Pubmed
Copeland LJ, Sneige N, Stringer CA, Gershenson DM, Saul PB, Kavanagh JJ (1985)
Alveolar rhabdomyosarcoma of the female genitalia.
Cancer 56: 849-55



5
 
Tavassoli FA, Devilee P (Eds.)
World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of the Breast and Female Genital Organs.
3rd Edition
IARC Press: Lyon 2003



.



Connective, subcutaneous and other soft tissues
ICD-O-3 topography code: C49
ICD10: C49
           

Rhabdomyosarcomas are the most frequent malignant soft tissue tumours in children and adolescents, with embryonal rhabdomyosarcoma as the most common subtype. Typical sites of involvement are the head and neck region and the genitourinary system. Phenotypically and biologically, embryonal rhabdomyosarcomas recapitulate features of embryonal skeletal muscle. Genetically, most cases show loss of chromosomal region 11p15
6
 
Alberto S. Pappo (Ed.)
Pediatric Bone and Soft Tissue Sarcomas
1st Edition
Springer Verlag: Berlin Heidelberg New York 2005



.

Three histological variants of embryonal rhabdomyosarcoma have been identified
7
 
Fletcher CDM, Unni KK, Mertens F (Eds.)
World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone.
3rd Edition
IARC Press: Lyon 2002



:

Spindle cell rhabdomyosarcoma
Botryoid rhabdomyosarcoma
Anaplastic rhabdomyosarcoma



Vagina
ICD-O-3 topography code: C52
ICD10: C52
           

Rhabdomyosarcomas are the most frequent malignant soft tissue tumours in children and adolescents, with embryonal rhabdomyosarcoma as the most common subtype. Typical sites of involvement are the head and neck region and the genitourinary system. Phenotypically and biologically, embryonal rhabdomyosarcomas recapitulate features of embryonal skeletal muscle. Genetically, most cases show loss of chromosomal region 11p15
8
 
Alberto S. Pappo (Ed.)
Pediatric Bone and Soft Tissue Sarcomas
1st Edition
Springer Verlag: Berlin Heidelberg New York 2005



.

Three histological variants of embryonal rhabdomyosarcoma have been identified
9
 
Fletcher CDM, Unni KK, Mertens F (Eds.)
World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone.
3rd Edition
IARC Press: Lyon 2002



:

Spindle cell rhabdomyosarcoma
Botryoid rhabdomyosarcoma
Anaplastic rhabdomyosarcoma



Cervix uteri
ICD-O-3 topography code: C53
ICD10: C53
           

Rhabdomyosarcomas are the most frequent malignant soft tissue tumours in children and adolescents, with embryonal rhabdomyosarcoma as the most common subtype. Typical sites of involvement are the head and neck region and the genitourinary system. Phenotypically and biologically, embryonal rhabdomyosarcomas recapitulate features of embryonal skeletal muscle. Genetically, most cases show loss of chromosomal region 11p15
10
 
Alberto S. Pappo (Ed.)
Pediatric Bone and Soft Tissue Sarcomas
1st Edition
Springer Verlag: Berlin Heidelberg New York 2005



.

Cervical embryonal rhabdomyosarcoma (sarcoma botryoides) typically grows in a polypoid fashion. The polypoid masses may be pedunculated or sessile. They range in size from 2-10 cm. Small haemorrhagig areas as well as islands of mature neoplastic cartilage may be observed.
Sarcoma botryoides is rare. It usually arises in children and young adults (mean age 18 years). The prognosis is better than for other types of cervical sarcoma
11
 
Tavassoli FA, Devilee P (Eds.)
World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of the Breast and Female Genital Organs.
3rd Edition
IARC Press: Lyon 2003



.