Hemihypertrophy and a poorly differentiated embryonal rhabdomyosarcoma of the pelvis

Medical and Pediatric Oncology

Volumn 32, Issue 1, 1999, Pages 38-43

  Samuel, David P ^a   Tsokos, Maria ^a   DeBaun, Michael R ^a,b  

^a NATIONAL CANCER INSTITUTE   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

11p15.5; Hemihypertrophy; LOH; MyoD1; Rhabdomyosarcoma; Sarcoma

Indexed keywords

ADOLESCENT; ADRENAL CORTEX CARCINOMA; ARTICLE; BECKWITH WIEDEMANN SYNDROME; CASE REPORT; CHROMOSOME 11P; CHROMOSOME ANALYSIS; EMBRYONAL RHABDOMYOSARCOMA; GIGANTISM; HEMIHYPERTROPHY; HEPATOBLASTOMA; HETEROZYGOSITY LOSS; HUMAN; HYPOGLYCEMIA; IMMUNOHISTOCHEMISTRY; KIDNEY MALFORMATION; MACROGLOSSIA; MALE; NEEDLE BIOPSY; NEPHROBLASTOMA; OMPHALOCELE; PRIORITY JOURNAL;

ADOLESCENT; CHROMOSOMES, HUMAN, PAIR 11; FATAL OUTCOME; FOOT DEFORMITIES, CONGENITAL; HUMANS; HYPERTROPHY; IMMUNOHISTOCHEMISTRY; LEG; LOSS OF HETEROZYGOSITY; LUNG NEOPLASMS; MALE; MYOD PROTEIN; PELVIC NEOPLASMS; RHABDOMYOSARCOMA, EMBRYONAL; TRANS-ACTIVATORS;

EID: 0032959785     PISSN: 00981532     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-911X(199901)32:1<38::AID-MPO8>3.0.CO;2-H     Document Type: Article

References (39)

1. Wagner H. Hypertrophie der rechten Brust und der rechten oberen Extremitat, besonders der Hand und den Fingeren. Med Jahrb KK Osterreichen Staates, 1839; 19:378-384.
2. Wakefield EG, Hines EA. Congenital hemihypertrophy: Report of 8 cases. Am J Med Sci 1933;185:493-498.
3. Ward J, Lerner HH. A review of the subject of congenital hemihypertrophy and a complete case report. J Pediatr 1947;31:403-414.
4. Ringrose RE, Jabbour JT, Keele DK. Hemihypertropy. Pediatrics 1965;36:434-448.
5. Parker DA, Skalkow RG. Congenital asymmetry: Report of 10 cases with developmental anomalies. Pediatrics 1969;44:584-589.
6. Gorlin RJ, Meskin LH. Congenital hemihypertyrophy. J Pediatr 1962;61:870-879.
7. Cohen MM Jr. A comprehensive and critical assessment of overgrowth and overgrowth syndromes. Adv Hum Genet 1989;18: 181-303.
8. Fraumeni JF, Geiser CF, Manning MD. Wilms tumor and congenital hemihypertrophy: Report of five new cases and review of literature. Pediatrics 1967;40:886-899.
9. Riedel HA. Adrenogenital syndrome in a male child due to adrenocortical tumor. Pediatrics 1952;10:19-27.
10. Roth F. Zur Kenntnis und Auffassung der Lebermischgeschwulste und des halbseitigen Risenwuchses. Frankfurt Z Path 1938;52: 163-196.
11. Lewis D, Geschickter CG. Tumors of the sympathetic nervous System. Arch Surg 1934;28:16-58.
12. Emery LG, Shields M, Shah N, et al. Neuroblastoma associated with Beckwith-Wiedemann syndrome. Cancer 1983;52:176-179.
13. Parra G, Seery W, Buchbinder M, et al. Congenital total hemihypertrophy and carcinoma of an undescended testicle: A case report. J Urol 1977;118:343-344.
14. Tomooka Y, Onitsuka H, Goya T, et al. Congenital hemihypertrophy with adrenal adenoma and medullary sponge kidney. Br J Radiol 1988;61:851-853.
15. Schnakenburg K, Muller M, Dorner K, et al. Congenital hemihypertrophy and malignant giant phaechromocytoma. A previously undescribed coincidence. Eur J Pediatr 1976;122:263-273.
16. Ruyman F, Maddux H, Ragab A, et al. Congenital anomalies associated rhabdomyosarcoma: An autopsy study of 115 cases. A report from the intergroup rhabdomyosarcoma study committee (representing the Children's Cancer Group, the Pediatric Oncology Group, the United Kingdom Children's Cancer Study Group and the Pediatric Intergroup Statistical Center). Med Pediatr Oncol 1988;16:33-39.
17. Seaver L, Hoyme E, Lyons-Jones K, et al. The incidence of neoplasia in children with isolated congenital hemihypertrophy: A twelve year experience. Proc Greenwood Genet Center Volume 12, 1993.
18. Besnard-Guerin C, Cavenee W, Newsham I. A highly polymorphic DNA restriction site marker in the 5′ region of the human tyrosine hydroxylase gene (TH) detecting loss of heterozygosity in human embryonal rhabdomyosarcoma. Hum Genet 1994;93: 349-350.
19. Barsky AJ. Macrodactyly. J Bone Joint Surg [Am] 1967;49:1255-1266.
20. Temtamy S, McKusick V. Macrodactyly as an isolated anomaly. Birth Defects 1978;14:507-511.
21. Temtamy S, McKusick V. Macrodactyly as part of a syndrome. Birth Defects 1978;14:522-524.
22. Pearn J, Viljoen D, Beighton P. Limb overgrowth - Clinical observations and nosological considerations. S Afr Med J 1983;84: 905-908.
23. Viljoen D, Pearn J, Beighton P. Manifestations and natural history of idiopathic hemihypertrophy: A review of eleven cases. Clin Genet 1984;26:81-86.
24. Stoll C, Alembik Y, Steib JP, et al. Twelve cases with hemihypertrophy: Etiology and follow-up. Genet Couns 1993;4:119-126.
25. Rowe NH, Hemifacial hypertrophy. Oral Surg 1962;15:575-587.
26. Carlin ME, Escobar LF, Ward RE, et al. A reassessment of Beckwith-Wiedemann syndrome. Am J Hum Genet 1990;47(suppl.):A50.
27. DeBaun MR, Tucker MA. Risk of cancer during the first four years of life in children from the Beckwith-Wiedemann Syndrome Registry. J Pediatr 1998;132:398-400.
28. Kousseff AL, Hermann J, Gilbert E, et al. Studies of malformation syndromes of man XXIX: The Beckwith-Wiedemann syndrome. Eur Pediatr 1976;123:139-166.
29. Barth RJ Jr, Merino MJ, Solomon D, et al. Prospective study of the value of core needle biopsy and fine needle aspiration in the diagnosis of soft tissue masses. Surgery 1994;112:536-543.
30. Koufos A, Hansen MF, Lampkin BC, et al. Loss of alleles at loci on human chromosome 11 during genesis of Wilms' tumour. Nature 1984;309:170-172.
31. Koufos A, Hansen MF, Copeland NG, el al. Loss of heterozygosity in three embryonal tumors suggests a common pathogenetic mechanism. Nature 1985;316:330-334.
32. Koufos A, Grundy P, Morgan K, et al. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5. Am J Hum Genet 1989;44:711-719.
33. Ping AJ, Reeve AE, Law DJ, et al. Genetic linkage of Beckwith-Wiedemann syndrome to 11p.15. Am J Hum Genet 1989;44:720-723.
34. Motou C, Junien C, Henry I, et al. Beckwith-Wiedemann syndrome: A demonstration of the mechanisms responsible for the excess of transmitting females. J Med Genet 1992;29:217-220.
35. Viljoen D, Ramesar R. Evidence for paternal imprinting in a familial Beckwith-Wiedemann syndrome. J Med Genet 1992;29: 221-225.
36. Dias P, Parham DM, Shapiro DN, et al. Myogenic regulatory protein (Myo Dl) expression in childhood solid tumors. Am J Pathol 1990;137:1283-1291.
37. Wang NP, Marx J, McNutt MA, et al. Expression of myogenic regulatory proteins (myogenin and MyoD1) in small blue round cell tumors of childhood. Am J Pathol 1995;147:1799-1810.
38. Scrabble H, Witte D, Shimada H, et al. Molecular differential pathology of rhabdomyosarcoma. Genes Chromosomes Cancer 1989;1:23-25.
39. Visser M, Sijmons C, Bras J, et al. Allelotype of pediatric rhabdomyosarcoma. Oncogene 1977;15:1309-1314.