Cancer mortality in relatives of desmoid sarcoma patients
DOI:
https://doi.org/10.32635/2176-9745.RBC.1990v36n1/4.3123Palavras-chave:
Sarcoma Desmóide, Mortalidade de Parentes no Sarcoma DesmóideResumo
Pacientes menores de 16 anos, com diagnóstico de sarcoma do tipo desmóide atendidos no Hospital M.D. Anderson da Universidade do Texas pelo período de 1944 e 1975, foram revistos. A mortalidade esperada foi calculada aplicando-se as taxas de mortalidade específicas por idade, raça e sexo dos Estados Unidos sobre a mortalidade pessoa/ano de risco observado. A razão da mortalidade padronizada - SMR - foi computada. Para o conjunto dos 429 parentes dos 26 casos de sarcoma do tipo desmóide aqui analisados, não foi encontrado excesso de mortes, observado/esperado = 13/24.7. O risco dos pais terem câncer também não foi significativo, observado/esperado = 2/1.83. Esses resultados são indicativos de que as taxas de mortalidade por este tipo de tumor, tanto para este grupo particular de famílias como para a população em geral, não são os parâmetros adequados para estudar fatores hereditários e ocorrência de tumores desmóides. Sugere-se a comparação de taxas de incidência de tumores benignos em tecidos moles entre os membros da familia dos casos com as taxas destes mesmos tumores na população em geral.
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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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