Cancer mortality in relatives of desmoid sarcoma patients

Authors

  • Louise C. Strong Head of the Department of Genetics from the University of Texas, Health Science Center. U.S
  • Anita Schnitman Department of Preventive Medicine, Federal University of Bahia. Salvador (BA), Brasil

DOI:

https://doi.org/10.32635/2176-9745.RBC.1990v36n1/4.3123

Keywords:

Desmoid Sarcoma, Relatives Mortality in Desmoid Sarcoma

Abstract

Desmoid sarcoma patients from the U.S. and Canada, diagnosed under the age of 16 years and referred to the University of Texas, M.D. Anderson Hospital - MDAH - between 1944 and 1975 were surveyed. Family information was collected for grandparents, parents, parental siblings, proband offspring and siblirtgs. Expected mortality was calculated by applying age-race-sex specific U.S. mortality rates to the person-years at risk. Standardized mortality ratio's - SMR- were calculated. Among 429 relatives of 26 desmoid sarcoma probands no overali cancer excess was found, observed/expected = 13/24.7. The risk among parents, the ones more informative for genetic analysis were also not significant, observed/expected = 2/1.83. An updated follow-up of incidence data of the study population and of the general population is suggested in the years to come, and in doing so, the inclusion of all familly members history should pull the results to a number closer to reality.

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References

ABRAMSON DH et al. Retreatment of retiriobiastoma with external beam irradiation. Arch Ophtalmol 1982; 100: 1257-1260. DOI: https://doi.org/10.1001/archopht.1982.01030040235004

ALLEN PW. The fibromatoses: A ciinicopathoiogical classification on 140 cases. Am J Surg Pathol 1977: 1255-270.

BAIRD AP. Congerutal generalized fibromatosis: An autossomal recessive condition? Clinical Genetics 1976; 9: 488-494. DOI: https://doi.org/10.1111/j.1399-0004.1976.tb01602.x

BARBER HM etal. – Multicentric extra-abdominal desmoid tumors. J Borie J Surg 1973; 55b: 858- 863. DOI: https://doi.org/10.1302/0301-620X.55B4.858

BARTLETT RC et al. - Multiple congenital neoplasms of 4 cases in one family. Cancer 1961; 14: 913-920. DOI: https://doi.org/10.1002/1097-0142(196109/10)14:5<913::AID-CNCR2820140503>3.0.CO;2-G

BOICE JD et al. - Epidemiologic analyses with a programmabie calculator - New edition with an appendix for HP-41CV by Hariand Austin School of Public Health, University of Alabama, Birmingham Boston: Epidemiology Resources Inc 1983.

BRASF1ELD RD et al. Desmoid tumors of the anterior abdominal wali. Surgery 1969; 65: 241-246.

CHAN H et al. A new familial cancer syndrome? A spectrum of malignant and bening tumors including retinobiastoma, and a probable case of multifocal osteosarcoma J Natl Cancer Lust 1977; 58: 205-207. DOI: https://doi.org/10.1093/jnci/58.2.205

CHUNG EB et al. infantile fibrosarcoma. Cancer 1976; 38: 729-730. DOI: https://doi.org/10.1002/1097-0142(197608)38:2<729::AID-CNCR2820380216>3.0.CO;2-Z

CONLEY J et al. Fibromatosis of the head and neck. Am J Surg 1966; 112: 609-614. DOI: https://doi.org/10.1016/0002-9610(66)90330-8

DAHN 1 et al. Desmoid tumors. Acta Chirurgica Scandinavica 1963; 126: 305.

DAS GUPTHA TK et al. Extra-abdominal desmoids – A clinicopathological Study. Am Surg 1969, 1970: 109-121. DOI: https://doi.org/10.1097/00000658-196907000-00012

DOMMISSE GF. Juvenile fibromatosis and other diseases of connective tissue. S Afri Med J 1979; 56: 1035-1040.

DRESCHER ES et al. Juvenile fibromatosis in sibiings. J Pediat Surg 1967; 2: 427-430. DOI: https://doi.org/10.1016/S0022-3468(67)80083-6

ENJOJI MN et al. Juvenile fibromatosis of the siblings. Acta Med Univ Kogoshima 1965; 10: 145-151.

ENZINGER FM et al. Musculoaponeurotic fibromatosis of the shouider-girdle extra abdominal. Cancer 1967; 20: 1131. DOI: https://doi.org/10.1002/1097-0142(196707)20:7<1131::AID-CNCR2820200716>3.0.CO;2-8

GESCHICKTER CF et al. Tumors of connective tissues. AJC 1935; 25: 630. DOI: https://doi.org/10.1158/ajc.1935.377

HAYRY P et al. Analysis of factors possibly contributing to the etiology and growth behavior. AJCP 1982; 6: 674-680. DOI: https://doi.org/10.1093/ajcp/77.6.674

HAYRY P et al. The desmoid tumor - 111. A biochemical and genetic analysis. AJCP 1982; 77: 681-685. DOI: https://doi.org/10.1093/ajcp/77.6.681

HILL DR et al. Radiation therapy of desmoid tumors. Am J Roentgenol Radium Ther Nuci Med 1973; 117: 84-89. DOI: https://doi.org/10.2214/ajr.117.1.84

HUTCHINSON RJ. Chemotherapy: A successtul application in abdominal fibromatosis. Pediatrics 1979; 63: 157-159. DOI: https://doi.org/10.1542/peds.63.1.157

JANNECK C. Contribution to a rare precancerous tumor in childhood. Baud 27, 1979; Helf 2: 130-135.

JYRKI JR. Incidence, sex-age and anatomical distribution in the finish population. AJCP. 1982; 77:665-673. DOI: https://doi.org/10.1093/ajcp/77.6.665

KELLEY JL et al. Desmoid tumors of the abdominal and thoracic walis in a chiid. Arch Surg 1960; 80: 144-150. DOI: https://doi.org/10.1001/archsurg.1960.01290180146018

KIRN DH et al. intra-abdominal desmoid tumor. Cancer 1971: 1041-1045. DOI: https://doi.org/10.1002/1097-0142(197105)27:5<1041::AID-CNCR2820270506>3.0.CO;2-E

KNUDSON AG Jr. etal. Heredity and cancer in man. Prog Me Genet 1973; 9: 113-157.

LIPSCHUTZ. Steroids hormones and tumor. Baltimore. The Williams and Wiikins Company, 1950.

LOWY M et al. Fibrome desmoid-transformation in fibrosarcoma. DermatologiCa 1981; 163: 125-136. DOI: https://doi.org/10.1159/000250149

MACKENZIE DH. The fibromatoses: A ciinicopathological concept. Br Med J 1972; 4: 277-281. DOI: https://doi.org/10.1136/bmj.4.5835.277

MCADAM WH et al. The occurrence of desmoid in patients with tamilial polyposis coli. Br J Surg 1970; 57: 618. DOI: https://doi.org/10.1002/bjs.1800570816

MCDOUGALL A et al. Extra abdominal desmoid tumors. J Bone Joint Surg 1979; 61 B: 373-377. DOI: https://doi.org/10.1302/0301-620X.61B3.479262

MONSON RR. Analyses of relative survival and proportiorial mortality. Comput Biom Res 1979; 7:325-332. DOI: https://doi.org/10.1016/0010-4809(74)90010-X

MUSGROVE JE et al. Extra-abdominal desmoid tumors: Their differential diagnosis and treatment. Arch Pathol 1948; 45: 513-540.

National Cancer for Health Statistics. Eighth Revision of the International Ciassification Diseases, Washington, D.C.: National Cancer for Health Statistics (Vital and Health Statistics) CDHEW publication no. 1693, 1968.

OBER WB et al. Desmoid tumor of polipteal space occurring space during pregnancy. Report of a case with bioassays. Journal of National Cancer institute 1955; 16: 569.

PEARMAN WO. Desmoid tumors. Ann Surg 1942; 114-125. DOI: https://doi.org/10.1097/00000658-194201000-00014

PFLUGER UH et al. Kongenitaie Polyfibromatose: Klinische und Genetische Untersuchungen. Wien Klin Wschr 1976; 88: 92-94.

RAGAB AH et al. Malignant tumors of soft tissues. Clinical Pediatric Oncoiogy. The CV Mosiey Company, 3rd Edition 1984: 660-661.

ROBBINS SL. Text Book of Pathological with Clinical Application. Philadelphia and London: W. B. Saunders Co. 1962: 1061.

SCH MIDT D et al. Fibromatosis of infancy and Chiidhood. Histology, Ultra Structure and Clinicopathologic Correlation. Z-Kiinderchir 1985; 40:40-46. DOI: https://doi.org/10.1055/s-2008-1059709

SCHRODER HA. Familial aggressive fibromatosis of the lower extremities. Acta Orthop Scand 1985; 56: 90-91. DOI: https://doi.org/10.3109/17453678508992990

SIEGAL A. et al. Aggressive fibromatosis (infantiie fibrosarcoma). Clin Ped 1978; 6: 517-520. DOI: https://doi.org/10.1177/000992287801700613

SMITH WG. Desmoid tumors in famiflal muitipie polyposis. Proc Mayo Clinic 1959; 34: 31-38.

SOULE EH et al. Fibrosarcoma in infants and chiidren. Cancer 1977; 40: 1711-1721. DOI: https://doi.org/10.1002/1097-0142(197710)40:4<1711::AID-CNCR2820400447>3.0.CO;2-9

STOUT AP. Fibrosarcoma in inlants and children. Cancer 1962: 15: 1028-1040. DOI: https://doi.org/10.1002/1097-0142(196209/10)15:5<1028::AID-CNCR2820150520>3.0.CO;2-X

STOUTAP. Juvenile fibromatosis. Cancer 1954; 7: 956. DOI: https://doi.org/10.1002/1097-0142(195409)7:5<953::AID-CNCR2820070520>3.0.CO;2-W

STRODE JE. Desmoid tumors particularly as related to their surgical removal. Ann Surg 1954; 139: 335. DOI: https://doi.org/10.1097/00000658-195403000-00011

STRONG LC et al. Cancer mortaiity in relatives of retinobiastoma patients. JNCI 1984; 73: 303-311. DOI: https://doi.org/10.1093/jnci/73.2.303

SWAIN RE et al. Fibrosarcoma of the head and neck in children. Laryngoscope 1976; 86: 113. DOI: https://doi.org/10.1288/00005537-197601000-00022

TENG P et al. Congenital generalized fibromatosis (renal and skeletal) with complete spontaneous regression. Pediat 1963; 62: 748-753. DOI: https://doi.org/10.1016/S0022-3476(63)80045-1

TOURAIN E A et al. La polyfibromatose hereditaire. Ann Derm Syp 5, 1-5, Paris.

TRIANTAFYLLON NM et al. Desmoid tumors of the bone. Int Surg 1972; 57: 793-797.

WADDEL WR. Treatment of intra-abdominal and abdominal wall desmoid tumors with drugs that affect metabolism of cyciic 3' 5' - Adenosine Mongshosphate. Ann Surg 1975; 181: 299-302. DOI: https://doi.org/10.1097/00000658-197503000-00009

WARA WM. Desmoid tumors - Treatment prognosis. Radiology 1977; 124: 225-226. DOI: https://doi.org/10.1148/124.1.225

WEE A et al. Infantile fibrosarcoma. Arch Pathol Lab Med 1979; 103: 236-238.

WHITFIELD A et al. Remarkabie series of molluscum fibrosum in children. Med Chir Trans 1903; 86: 293-301.

WILLIAMS JO et al. Congenital fibrosarcoma. Arch Patha (Chic) 1951; 51: 548-552.

YOUNG ID et al. Familial fibromatosis. Clinical Genetics 1981; 20: 221-2 16. DOI: https://doi.org/10.1111/j.1399-0004.1981.tb01831.x

ZAYID letal. Familial muiticentric tibromatosis desmoids. A report of three cases in aJordanianfamiiy. Cancer 1969: 24: 786-795. DOI: https://doi.org/10.1002/1097-0142(196910)24:4<786::AID-CNCR2820240420>3.0.CO;2-0

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Published

2023-07-31

How to Cite

1.
Strong LC, Schnitman A. Cancer mortality in relatives of desmoid sarcoma patients. Rev. Bras. Cancerol. [Internet]. 2023 Jul. 31 [cited 2024 Nov. 22];36(1/4):45-8. Available from: https://rbc.inca.gov.br/index.php/revista/article/view/3123

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ORIGINAL ARTICLE