Health Dictionary

Overview

The origin of rhabdomyosarcoma is straited muscle cells.The presentation sites of rhabdomyosarcoma are head and neck, extremities, Genitourinary tract, trunk, orbit, retroperitoneum, bladder, vagina, nasopharynx, and middle ear.The exact pathogenesis of rhabdomyosarcoma is unclear. However, there is causal association between MET proto-oncogene and macrophage migration inhibitory factor (MIF) and it is thought that P53 is related to oncogenic transformation and tumor progression. Multiple gene mutations are related to rhabdomyosarcoma such as loss of heterozygosity of 11p15, TP53, NRAS, KRAS, HRAS, PIK3CA, CTNNB1, FGFR4, and translocation in PAX3 or PAX7 genes with FOXO1. Immunohistochemistry can identify some specific proteins related to rhabdomyosarcoma such as desmin, actin, myogenin, and myoglobin. The other histologic procedure is transmission electron microscopy (TEM) which can be used for poorly differentiated or undifferentiated tumors and myofilaments, actin, desmin, myotubular intermediate filaments, and rudimentary Z-band material. Fusion protein is identified by reverse transcriptase polymerase chain reaction and fluorescent in situ hybridization.

Pathophysiology

Histology

The origin of rhabdomyosarcoma is straited muscle cells.^[1]
The presentation sites of rhabdomyosarcoma are:
- Head and neck (28%)
- Extremities (24%)
- Genitourinary tract (18%)
- Trunk (11%)
- Orbit (7%)
- Retroperitoneum (6%)
- Other sites such as bladder, vagina, nasopharynx, and middle ear (3%)
Round or spindle-shaped muscle cells are present in embryonal rhabdomyosarcoma (ERMS).^[2]
Alveolar architecture with small round undifferentiated cells which are separated by dense hyalinized fibrous septa are present in alveolar rhabdomyosarcoma (ARMS).
Despite all muscle differentiation markers expression in ARMS, mature muscle characteristics is not seen in ARMS histology.

Pathogenesis

The exact pathogenesis of rhabdomyosarcoma is unclear.^[3]
Distruption of skeletal muscle progenitor cell growth and related differentiation may cause rhabdomyosarcoma.^[3]
There is causal association between MET proto-oncogene and macrophage migration inhibitory factor (MIF).^[4]
It is thought that P53 is related to oncogenic transformation and tumor progression.^[5]

Genetics

According to microarray and targeted sequencing, following genomic characteristics are attributed to Rhabdomyosarcoma (RMS):^[6]^[7]^[8]^[9]^[10]^[11]
- Loss of heterozygosity of 11p15.
- Mutations in TP53
- Mutations in NRAS
- Mutations in KRAS
- Mutations in HRAS
- Mutations in PIK3CA
- Mutations in CTNNB1
- Mutations in FGFR4
- Translocations in PAX3 or PAX7 genes with FOXO1
Specific genetic changes in different types of rhabdomyosarcoma:
Alveolar rhabdomyosarcoma:^[12]^[13]
- Translocation of FKHR gene on chromosome 13 with the PAX3 gene on chromosome 2 or the PAX7 gene on chromosome 1
- PAX7 translocation occur in younger patients with longer event-free survival rate
Embryonal rhabdomyosarcoma:^[14]
- Particular gene changes are not clear
- Loss of heterozygosity from the 11p15 region
- Hyperdiploid gene
- Lack of gene amplification

Associated conditions

Immunohistochemistry

Through immunohistochemistry, muscle specific proteins can be identified in RMS.^[2]
RMS stains positive for following proteins:
- Polyclonal desmin (99%)
- Muscle-specific actin (95%)
- Myogenin or myogenic differentiation 1 ( MyoD1) (95%)
  - Expressed more in ARMS rather than ERMS
  - Associated with poorer prognosis
- Myoglobin (78%)

Transmission electron microscopy

Transmission electron microscopy (TEM) can be used for poorly differentiated or undifferentiated tumors.^[15]^[16]
Presence of following proteins are associated with TEM features of RMS:
- Myofilaments
- Desmin and actin filaments
- Myotubular intermediate filaments
- Rudimentary Z-band material

Reverse transcriptase polymerase chain reaction (RT-PCR)

Fluorescent in situ hybridization (FISH)

By using RT-PCR and FISH, features of fusion protein are identified in ARMS.^[17]

Gross Pathology


Gross findings	Gross pathology
Clusters of edematous and grape-like masses Protrusion into lumen of hollow organs
Poorly circumscribed mass white and infiltrative soft or firm mass	Gross feature of orbital embryonal rhabdomyosarcoma Source: Contributed by Mark R. Wick, M.D., from Pathologyoutlines
Fleshy tumor Tan gray color tumor	Gross pathology of alveolar rhabdomyosarcoma Source:Courtesy of Mark R. Wick, M.D., from Pathologyoutlines

Microscopic Pathology


Pathologic findings	Microscopic pathology
The microscopic features of ARMS are:^[18] Ovoid to round tumor cells are packed with fibrovascular septae Tumor cells have club-shaped appearance Tumor cells are divided by pseudo-alveolar spaces, slightly like pulmonary alveoli Rhabdomyoblasts are shed into pseudo-alveolar areas Presence of more than 50% alveolar components	Alveolar Rhabdomyosarcoma- intermediate magnification Source: Nephron,from Wikimedia Commons
The microscopic features of ERMS are:^[14]^[19] Rhabdomyoblasts arranged in sheets and large nests Different stages of cell morphogenesis Positive stains are desmin, actin, myogenin, and MyoD1 Infrequent intermixed fusiform cells No alveolar architectural pattern Typical rhabdomyoblast has eosinophilic cytoplasm with poorly formed myofilaments	Microscopic pathology of embryonal rhabdomyosarcoma Source: Contributed by Mark R. Wick, M.D., from Pathologyoutlines
The microscopic features of botryoid rhabdomyosarcoma:^[20] Botryoid rhabdomyosarcoma grows beneath an epithelial surface Rhabdomyoblasts adhere to dense subepithelial which is called cambrium layer Malignant cells are found in myoxid stroma	Microscopic feature of botryoid rhabdomyosarcoma from Pathologyoutlines
The microscopic features of anaplastic rhabdomyosarcoma are:^[21] Presence of large hyperchromatic nuclei Atypical bizarre mitotic features Threefold larger nuclear size	Microscopic feature of anaplastic rhabdomyosarcoma from Pathologyoutlines

References

↑ Barr FG (1997). “Molecular genetics and pathogenesis of rhabdomyosarcoma”. J Pediatr Hematol Oncol. 19 (6): 483–91. PMID 9407933.
↑ ^2.0 ^2.1 Dias P, Chen B, Dilday B, Palmer H, Hosoi H, Singh S; et al. (2000). “Strong immunostaining for myogenin in rhabdomyosarcoma is significantly associated with tumors of the alveolar subclass”. Am J Pathol. 156 (2): 399–408. doi:10.1016/S0002-9440(10)64743-8. PMC 1850049. PMID 10666368.
↑ ^3.0 ^3.1 Taulli R, Scuoppo C, Bersani F, Accornero P, Forni PE, Miretti S; et al. (2006). “Validation of met as a therapeutic target in alveolar and embryonal rhabdomyosarcoma”. Cancer Res. 66 (9): 4742–9. doi:10.1158/0008-5472.CAN-05-4292. PMID 16651427.
↑ Tarnowski M, Grymula K, Liu R, Tarnowska J, Drukala J, Ratajczak J; et al. (2010). “Macrophage migration inhibitory factor is secreted by rhabdomyosarcoma cells, modulates tumor metastasis by binding to CXCR4 and CXCR7 receptors and inhibits recruitment of cancer-associated fibroblasts”. Mol Cancer Res. 8 (10): 1328–43. doi:10.1158/1541-7786.MCR-10-0288. PMC 2974061. PMID 20861157.
↑ Xu J, Timares L, Heilpern C, Weng Z, Li C, Xu H; et al. (2010). “Targeting wild-type and mutant p53 with small molecule CP-31398 blocks the growth of rhabdomyosarcoma by inducing reactive oxygen species-dependent apoptosis”. Cancer Res. 70 (16): 6566–76. doi:10.1158/0008-5472.CAN-10-0942. PMC 2922473. PMID 20682800.
↑ Scrable H, Cavenee W, Ghavimi F, Lovell M, Morgan K, Sapienza C (1989). “A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting”. Proc Natl Acad Sci U S A. 86 (19): 7480–4. PMC 298088. PMID 2798419.
↑ Taylor AC, Shu L, Danks MK, Poquette CA, Shetty S, Thayer MJ; et al. (2000). “P53 mutation and MDM2 amplification frequency in pediatric rhabdomyosarcoma tumors and cell lines”. Med Pediatr Oncol. 35 (2): 96–103. PMID 10918230.
↑ Stratton MR, Fisher C, Gusterson BA, Cooper CS (1989). “Detection of point mutations in N-ras and K-ras genes of human embryonal rhabdomyosarcomas using oligonucleotide probes and the polymerase chain reaction”. Cancer Res. 49 (22): 6324–7. PMID 2680062.
↑ Shukla N, Ameur N, Yilmaz I, Nafa K, Lau CY, Marchetti A; et al. (2012). “Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcoma and neuroblastoma with mutated genes in growth signaling pathways”. Clin Cancer Res. 18 (3): 748–57. doi:10.1158/1078-0432.CCR-11-2056. PMC 3271129. PMID 22142829.
↑ Taylor JG, Cheuk AT, Tsang PS, Chung JY, Song YK, Desai K; et al. (2009). “Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models”. J Clin Invest. 119 (11): 3395–407. doi:10.1172/JCI39703. PMC 2769177. PMID 19809159.
↑ Barr FG, Galili N, Holick J, Biegel JA, Rovera G, Emanuel BS (1993). “Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma”. Nat Genet. 3 (2): 113–7. doi:10.1038/ng0293-113. PMID 8098985.
↑ Missiaglia E, Williamson D, Chisholm J, Wirapati P, Pierron G, Petel F; et al. (2012). “PAX3/FOXO1 fusion gene status is the key prognostic molecular marker in rhabdomyosarcoma and significantly improves current risk stratification”. J Clin Oncol. 30 (14): 1670–7. doi:10.1200/JCO.2011.38.5591. PMID 22454413.
↑ Cao L, Yu Y, Bilke S, Walker RL, Mayeenuddin LH, Azorsa DO; et al. (2010). “Genome-wide identification of PAX3-FKHR binding sites in rhabdomyosarcoma reveals candidate target genes important for development and cancer”. Cancer Res. 70 (16): 6497–508. doi:10.1158/0008-5472.CAN-10-0582. PMC 2922412. PMID 20663909.
↑ ^14.0 ^14.1 Invalid <ref> tag; no text was provided for refs named pmid94079332
↑ Hicks J, Flaitz C (2002). “Rhabdomyosarcoma of the head and neck in children”. Oral Oncol. 38 (5): 450–9. PMID 12110339.
↑ Parham DM (2001). “Pathologic classification of rhabdomyosarcomas and correlations with molecular studies”. Mod Pathol. 14 (5): 506–14. doi:10.1038/modpathol.3880339. PMID 11353062.
↑ Helman LJ, Meltzer P (2003). “Mechanisms of sarcoma development”. Nat Rev Cancer. 3 (9): 685–94. doi:10.1038/nrc1168. PMID 12951587.
↑ Hostein I, Andraud-Fregeville M, Guillou L, Terrier-Lacombe MJ, Deminière C, Ranchère D; et al. (2004). “Rhabdomyosarcoma: value of myogenin expression analysis and molecular testing in diagnosing the alveolar subtype: an analysis of 109 paraffin-embedded specimens”. Cancer. 101 (12): 2817–24. doi:10.1002/cncr.20711. PMID 15536621.
↑ Qualman SJ, Coffin CM, Newton WA, Hojo H, Triche TJ, Parham DM; et al. (1998). “Intergroup Rhabdomyosarcoma Study: update for pathologists”. Pediatr Dev Pathol. 1 (6): 550–61. PMID 9724344.
↑ Neha B, Manjunath AP, Girija S, Pratap K (2015). “Botryoid Rhabdomyosarcoma of the Cervix: Case report with review of the literature”. Sultan Qaboos Univ Med J. 15 (3): e433–7. doi:10.18295/squmj.2015.15.03.022. PMC 4554283. PMID 26357564.
↑ Hettmer S, Archer NM, Somers GR, Novokmet A, Wagers AJ, Diller L; et al. (2014). “Anaplastic rhabdomyosarcoma in TP53 germline mutation carriers”. Cancer. 120 (7): 1068–75. doi:10.1002/cncr.28507. PMC 4173134. PMID 24382691.

[pmid9407933-1] Barr FG (1997). “Molecular genetics and pathogenesis of rhabdomyosarcoma”. J Pediatr Hematol Oncol. 19 (6): 483–91. PMID 9407933.

[pmid10666368-2] 2.0 ^2.1 Dias P, Chen B, Dilday B, Palmer H, Hosoi H, Singh S; et al. (2000). “Strong immunostaining for myogenin in rhabdomyosarcoma is significantly associated with tumors of the alveolar subclass”. Am J Pathol. 156 (2): 399–408. doi:10.1016/S0002-9440(10)64743-8. PMC 1850049. PMID 10666368.

[pmid16651427-3] 3.0 ^3.1 Taulli R, Scuoppo C, Bersani F, Accornero P, Forni PE, Miretti S; et al. (2006). “Validation of met as a therapeutic target in alveolar and embryonal rhabdomyosarcoma”. Cancer Res. 66 (9): 4742–9. doi:10.1158/0008-5472.CAN-05-4292. PMID 16651427.

[pmid20861157-4] Tarnowski M, Grymula K, Liu R, Tarnowska J, Drukala J, Ratajczak J; et al. (2010). “Macrophage migration inhibitory factor is secreted by rhabdomyosarcoma cells, modulates tumor metastasis by binding to CXCR4 and CXCR7 receptors and inhibits recruitment of cancer-associated fibroblasts”. Mol Cancer Res. 8 (10): 1328–43. doi:10.1158/1541-7786.MCR-10-0288. PMC 2974061. PMID 20861157.

[pmid20682800-5] Xu J, Timares L, Heilpern C, Weng Z, Li C, Xu H; et al. (2010). “Targeting wild-type and mutant p53 with small molecule CP-31398 blocks the growth of rhabdomyosarcoma by inducing reactive oxygen species-dependent apoptosis”. Cancer Res. 70 (16): 6566–76. doi:10.1158/0008-5472.CAN-10-0942. PMC 2922473. PMID 20682800.

[pmid2798419-6] Scrable H, Cavenee W, Ghavimi F, Lovell M, Morgan K, Sapienza C (1989). “A model for embryonal rhabdomyosarcoma tumorigenesis that involves genome imprinting”. Proc Natl Acad Sci U S A. 86 (19): 7480–4. PMC 298088. PMID 2798419.

[pmid10918230-7] Taylor AC, Shu L, Danks MK, Poquette CA, Shetty S, Thayer MJ; et al. (2000). “P53 mutation and MDM2 amplification frequency in pediatric rhabdomyosarcoma tumors and cell lines”. Med Pediatr Oncol. 35 (2): 96–103. PMID 10918230.

[pmid2680062-8] Stratton MR, Fisher C, Gusterson BA, Cooper CS (1989). “Detection of point mutations in N-ras and K-ras genes of human embryonal rhabdomyosarcomas using oligonucleotide probes and the polymerase chain reaction”. Cancer Res. 49 (22): 6324–7. PMID 2680062.

[pmid22142829-9] Shukla N, Ameur N, Yilmaz I, Nafa K, Lau CY, Marchetti A; et al. (2012). “Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcoma and neuroblastoma with mutated genes in growth signaling pathways”. Clin Cancer Res. 18 (3): 748–57. doi:10.1158/1078-0432.CCR-11-2056. PMC 3271129. PMID 22142829.

[pmid19809159-10] Taylor JG, Cheuk AT, Tsang PS, Chung JY, Song YK, Desai K; et al. (2009). “Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models”. J Clin Invest. 119 (11): 3395–407. doi:10.1172/JCI39703. PMC 2769177. PMID 19809159.

[pmid8098985-11] Barr FG, Galili N, Holick J, Biegel JA, Rovera G, Emanuel BS (1993). “Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma”. Nat Genet. 3 (2): 113–7. doi:10.1038/ng0293-113. PMID 8098985.

[pmid22454413-12] Missiaglia E, Williamson D, Chisholm J, Wirapati P, Pierron G, Petel F; et al. (2012). “PAX3/FOXO1 fusion gene status is the key prognostic molecular marker in rhabdomyosarcoma and significantly improves current risk stratification”. J Clin Oncol. 30 (14): 1670–7. doi:10.1200/JCO.2011.38.5591. PMID 22454413.

[pmid20663909-13] Cao L, Yu Y, Bilke S, Walker RL, Mayeenuddin LH, Azorsa DO; et al. (2010). “Genome-wide identification of PAX3-FKHR binding sites in rhabdomyosarcoma reveals candidate target genes important for development and cancer”. Cancer Res. 70 (16): 6497–508. doi:10.1158/0008-5472.CAN-10-0582. PMC 2922412. PMID 20663909.

[pmid94079332-14] 14.0 ^14.1 Invalid <ref> tag; no text was provided for refs named pmid94079332

[pmid12110339-15] Hicks J, Flaitz C (2002). “Rhabdomyosarcoma of the head and neck in children”. Oral Oncol. 38 (5): 450–9. PMID 12110339.

[pmid11353062-16] Parham DM (2001). “Pathologic classification of rhabdomyosarcomas and correlations with molecular studies”. Mod Pathol. 14 (5): 506–14. doi:10.1038/modpathol.3880339. PMID 11353062.

[pmid12951587-17] Helman LJ, Meltzer P (2003). “Mechanisms of sarcoma development”. Nat Rev Cancer. 3 (9): 685–94. doi:10.1038/nrc1168. PMID 12951587.

[pmid15536621-18] Hostein I, Andraud-Fregeville M, Guillou L, Terrier-Lacombe MJ, Deminière C, Ranchère D; et al. (2004). “Rhabdomyosarcoma: value of myogenin expression analysis and molecular testing in diagnosing the alveolar subtype: an analysis of 109 paraffin-embedded specimens”. Cancer. 101 (12): 2817–24. doi:10.1002/cncr.20711. PMID 15536621.

[pmid9724344-19] Qualman SJ, Coffin CM, Newton WA, Hojo H, Triche TJ, Parham DM; et al. (1998). “Intergroup Rhabdomyosarcoma Study: update for pathologists”. Pediatr Dev Pathol. 1 (6): 550–61. PMID 9724344.

[pmid26357564-20] Neha B, Manjunath AP, Girija S, Pratap K (2015). “Botryoid Rhabdomyosarcoma of the Cervix: Case report with review of the literature”. Sultan Qaboos Univ Med J. 15 (3): e433–7. doi:10.18295/squmj.2015.15.03.022. PMC 4554283. PMID 26357564.

[pmid24382691-21] Hettmer S, Archer NM, Somers GR, Novokmet A, Wagers AJ, Diller L; et al. (2014). “Anaplastic rhabdomyosarcoma in TP53 germline mutation carriers”. Cancer. 120 (7): 1068–75. doi:10.1002/cncr.28507. PMC 4173134. PMID 24382691.

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