75.1ª.07 BIBLIOGRAFIA.

 

                                                   

   Capítulo 1. Introducción.

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  • Kransdorf M, Murphey M. Origin and classification of soft tissue tumors. In: Kransdorf M, Murphey M (Eds), Imaging of Soft Tissue Tumors. 2nd.Ed. Philadelphia: Lippincott Williams & Wilkins; 2006. pp 1-5.
  • Kransdorf M, Murphey M. Soft tissue tumors in a large referral population: prevalence and distribution of diagnoses by age, sex and location. In: Kransdorf M, Murphey M (Eds), Imaging of Soft Tissue Tumors. 2nd.Ed. Philadelphia: Lippincott Williams & Wilkins; 2006. pp 6-37.
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  • Vals O, Marinello Z, Paramio A: Tumores y lesiones seudotumorales de partes blandas. Madrid: España 1975;126-1277.

                                              

   Capítulo 2. Tumores adipociticos de localizacion cervical.

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  • Blanco ME, Perez A, Kofman S, Zenteno JC. Clinical and cytogenetic findings in 14 patients with madelung anomaly. Orthopedics 2005; 28: 315-319.
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  • Cox RW. Hibernoma: the lipoma of immature adipose tissue. Journal of Pathology and Bacteriology, 1954;68: 511-518.
  • Chan ES, Ahuha AT, King AD, Lau WY. Head and Neck cancers associated with Madelung?s disease. Ann Surg Oncol 1999;6(4):395-7.
  • Darsonval V, Duly T, Munin O, Houet JF. Surgical tratment of Launois - Bensaude disease, The value of liposuction. Ann Chir Plast Esthet 1990;35(2):128-33.
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  • Della Volpe C, Salazard B, Casanova D, Vacheret H, Bartoli JF, Magalon G. Hibernoma of the anterolateral thig. BJPS 2005; 58: 859-861.
  • Dardick I. (1978) Hibernoma: A possible model of brown fat histogenesis. Human Pathology, 1978;9: 321-329.
  • Enterline HT, Lowry LD, Richman AV. (1979) Does malignant hibernoma exist? American Journal of Surgical Pathology, 1979;3:265-271.
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  • Enzi G, Biondetti PR, Fiore D, et al. Multiple symmetrical lipomatosis: an updated clinical report. Medicine 1984;63:56.
  • Enzi G, Ageline C, Negrin P, Armani M, Pierobon S, Fedel D. Sensory, motor, and autonomic neuropathy in patients with multiple symmetric lipomatosis. Medicine 1986; 64:388-393.
  • Enzi G, Busetto L, Ceschin E, Coin A, Digito M. and Pigozzo S. Multiple symmetrix lipomatosis: Clinical aspects and outcome in a long-term longitudinal study. Int J Obes 2002; 26:253-261.
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  • Faga A, Valdatta LA, Thione A, Buoro M. Ultrasound Assisted liposuction for the palliative treatment of Madelung´s Disease: A case report. Aesthet Plast Surg 2001; 25: 181-183.
  • Fagan JJ, Myers EN, Barnes L. A parapharyngeal myxoid liposarcoma. The Journal of Laryngology and Otology 1999; 113:179-182.
  • Feldman DR, Schabel SI. Mulytiple symmetrical lipomatosis: computed tomographic appearance. South Med J 1995;88(6):681-2.
  • Fentinman IS, Davies EE, Ramsay GS. Hibernoma of the thigh. Clinical Oncology, 1975;1:71-76.
  • Fernández Fernández L, Hondler C, Tejero E, Pellicer JL, Ratia T, Alfaro J, Tieso A, Yagüe S. Liposarcoma bien diferenciado de tipo lipomatoide localizado en cuello y mediastino. Cirugía Española 1991;3:266-268.
  • Florio G, Cicia S, Del Papa M, Carni D. Neck hibernoma: case report and literature review. G Chir 2000; 21(8-9):339-41.
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  • Furlong MA, Fanburg-Smith JC, Miettinen M. The Morphologic spectrum of hibernoma: a clinicopathologic study of 170 cases. Am J Surg Pathol 2001; 25: 809-814.
  • Gialdini F, Frezza D, Alaggio R, Biscaro G. Liposarcoma del cavo orale: descrizione di un caso e revisione della letteratura. Acta Otorhinol Ital 1995; 15: 112-116.
  • Golledge J, Fisher C, Rhys-Evans Ph. Head and Neck Liposarcoma. Cancer 1995;76: 1051-58.
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  • Hany TF, Gharehpapagh E, Kamel EM, Buck A, Himms-Hagen J, von Schulthess GK. Brown adipose tissue: a factor to consider in symmetrical tracer uptake in the neck and upper chest region. Eur J Nucl Med Mol Imaging 2002; 29:1393.
  • Hull D. The structure and function of brown adipose tissue. British Medical Bulletin, 1966;22:92-93.
  • Josephson GD, Sclafani AP, Stern J. Benign symmetrical lipomatosis (Madelun’s disease). Otolaryngol Head Neck Surg 1996;115:170.
  • Kallas KM, Vaughan L, Haghighi P, Resnick D: Hibernoma of the left axilla; a case report and review of MRI imaging. Skeletal Radiol 2003;32: 290-294.
  • Kindblom LG, Svensson U. Multiple hibemomas of the heart. A case report. Acta Pathologica Microbiologica Scandinavica. Section A: Pathology, 1977;85: 122-126.
  • Kohan D, Miller PJ, Rothstein SG, Kaufman D. Madelung’s disease: case reports and literature review. Otolaryngol Head Neck Surg 1993;108:156-9.
  • Kransdorf MJ. Malignant Soft-Tissue tumors in a Large Referral Population: Distribution of Diagnoses by Age, Sex, and Location. AJR 1995; 164:129-134.
  • Kraus MD, Guillou L, Fletcher CD. Well Differentiated inflammatory liposarcoma an uncommon and easily overlooked variant of a common sarcoma. Am J Surg Pathol 1997; 21:518-27.
  • Launois PE, Bensaude R. De l’adeno-lipomatose symetrique. Bull Soc Med Hop Paris 1898;1:298-318.
  • Lawson W, Biller HF. Cervical Hibernoma. Laryngoscopie, 1976;86:1258-1267.
  • Lee JC , Gupta A, Saifuddin A, Flanagan A, Skinner JA, Briggs TWR, Cannon SR. Hibernoma: MRI features in eight consecutive cases. Clin Radiol 2006 61:1029-1034.
  • Leung NW, Gaer J, Beggs D, et al. Multiple symmetrical lipomatosis-effect of oral salbutamol. Clin Endocrinol 1987;27:601.
  • Loke TKL, Yung K, Chow TL, Lo S, Chan CS. Multiple symmetric lipomatosis in Chinese: Ultrasound, CT and MR Imaging. Clin Radiol 1998; 53: 903-906.
  • Madelung OW. Uber den Fetthals (diffuses Lipom des Halses). Langenbecks Arch Klin Chir 1888;37:106-30.
  • Mandell DL, Brandwein MS, Woo P, Som Pm, Biller HF, Urken ML. Upper Aerodigestive Tract Liposarcoma: Report on Four Cases and Literature Review. Laryngoscope 1999; 109: 1245-1252.
  • Matamala C, Perez JI, Amores H. Multiple symmetric lipomatosis. An Med Interna 1994; 11: 95-99.
  • Mclane RC, Meyer LC. Axillary Hibernoma: Review of the literature with report of a case examined angiographically. Radiology, 1978;127:673-674.
  • Mesera BW, Batsakis JG. Hibernoma of the neck. Archives of Otolaryngology, 1976;85: 199-201.
  • Mo L, Xu J, Yang R, Li S, Yang J, Li W. Benign symmetric lipomatosis. Lin Chuang Er Bi Yan Hou Ke Za Zhi 2002; 16:537-538.
  • Mouret P. Liposarcome de l’hypopharynx. A propos d’un cas avec revue de la littérature. Rev Laryngol Otol Rhinol 1999; 120: 39-42.
  • Muñoz A, Bautista J, Salazar JA, Aguilera I, García R, Chinchon I et al. Lipomatosis, proximal myopathy, and the mitochondrial 8344 mutation. A lipid storage myopathy? Muscle Nerve 2000; 23: 538-542.
  • Muñoz C, Aladro Y, Conde, Campos Y, Arenas J. Multiple symmetrical lipomatosis with familial polineuropathy. Rev Neurol 2001; 32: 1107-1111.
  • Mustafa K.SEM, Metin KARAK.K. Hibernoma: A case report and discussion of a rare tumor. Turk J Med Sci 2001; 25:175-176.
  • Napolitana L. The fine structure of adipose tissues. In: Renold, AE, Cahill GF. (eds.) Handbook of physiology, Section 5: Adipose tissue, pp. 109-110. American Physiological Society, Washington. 1965.
  • Napolitano L, Fawcett D. The fine structure of brown adipose tissue in the newborn mouse and rat. Journal of Biophysiology, Biochemistry and Cytology 1958;4: 685-696.
  • Nielsen S, Levine J, Clay R, Jensen M. Adipose tissue metabolism in benign symmetric lipomatosis. J Clin Endocrinol Metab 2001; 86: 2717-2720.
  • Novy CG, Wilson C. Hibernomas, brown fat tumours. Archives of Dermatology, 1956;73:149-151.
  • Otte TH. Liposarcoma of the Head and Neck. Archives of Otorhinolaryngology 1981;232: 285-291.PinsKy KS, Roenigk HH Jr. Liposuction of lipomas. Dermatol Clin 1990; 8: 483-492.
  • Rasmussen AT. The so-called hibernating gland. Journal of Morphology, 1923;38: 147-205.
  • Reitan JB, Kaafhus O, Brennhoud IO, Sager EM, Stenwing AE, Talle K. Pronostic factors in liposarcoma. Cancer 1985; 55: 2482-2490.
  • Rodríguez C, Díaz R, Fernández R, Teijeira S, Fachal C. Lipomatosis simétrica múltiple: Aportación de un caso y revisión de la literatura. Rev Intern Dermatol Dermocosm Clínica 2001; 4: 467-471.
  • Rosai J, Rosai and Ackerman´s Surgical Pathology. Soft Tissues. 9th Edition. 2004. 25: 2279.
  • Ruiz Liso JM, Sanz Anquela JM, Arrinda Yeregui JM, Gimeno Esteras E. Liposarcoma mixoide de ala nasal. Actas Dermo-Sif 1987;6:417-420.
  • Ruzicka T, Vieluf D, Landthaler M, et al. Benign symmetrical lipomatosis. J Am Acad Dermatol 1987;17:663-74.
  • Saddik M, Oldring DJ, Mourad WA. Liposarcoma of the Base of Tongue and Tonsillar Fossa. A Possibly Underdiagnosed Neoplasm. Arch Pathol Lab Med 1996; 120: 292-295.
  • Seemayer TA, Knaack J, Wang NS, Ahmed MN. On the ultrastructure of hibernoma. Cancer, 175;36:1785-1793.
  • Sidman RL. Histogenesis of brown adipose tissue in vivo and in organ culture. Anatomical Record, 1956;Y2A;581-585.
  • Smith PD, Stadelmann WK, Wassermann RJ, Kearney RE. Benign symmetric lipomatosis (Madelung’s disease). Ann Plast Surg 1998;41(6):671-3.
  • Smon HE. (1950) Posterior cervical tumor of brown fat in man: Its relationship to the interscapular gland of hibernating animals. American Journal of Surgery, 1950;80: 127-130.
  • Spano JP, Taillibert S, Khayat D, Terrier P. Hibernoma, an uncommon tumor as a differential diagnosis of liposarcoma of the thigh. Anticancer Res 2000;20(6C): 4803-4.
  • Suangshoti S, Menakanit W. Intraspinal hibernoma. British Journal of Surgery, 1974;61: 580-582.
  • Stewart MG, Schwartz MR, Alford BR. Atypical and Malignant Lipomatous Lesions of the Head and Neck. Arch Otolaryngol Head Neck Surg 1994; 120: 1151-1155.
  • Subramaniam RM, Clayton AC, Karantanis D, Collins DA. Hibernoma: 18FDG PET/CT Imaging. J Thoracic Oncol 2007 , 2:569-570.
  • Teplisky V, Huminer D, Dux S, Learmen Y, Zoldan J, Pitlik SD. Multiple symmetric lipomatosis presenting with polyneuropathy. Irs J Med Sci 1995;31:693-695.
  • Tizes R, Tizes BR. Lipo-hibernoma: Report of an unusual case. Angiology, 1974;25:228-230.
  • Tizian C, Berger A, Vykoupil KF. Malignant degeneration in Madelung’s disease (benign lipomatosis of the Neck). Br J Plastic Surg 1983;36(2):187-9.
  • Topalo VM. Benign symmetric lipomatosis localized mainly in the region of the neck (Madelung´s disease). Chirurgia 1992; 3: 26-32.
  • Uglesic V, Knezevic P, Milic M, Jokic D, Kosutic D. Madelung syndrome (benign lipomatosis): clinical course and treatment. Scand J Plast Reconstr Surg Hand Surg 2004;38: 240-243.
  • Vidal N, Torche M, Urquieta K, Lanzarini E. Hibernoma. Presentación de dos casos clínicos. Rev Chil Cirg 2004;56:279-282.
  • Vinayak BC, Reddy KT. Hibernoma in the parotid region. J Laryngol Otol 1993;107: 257-8.
  • Worsey J, McGuirt W, Carrau RL, Peitzman AB. Hiberoma of the neck: a rare cause of neck mass. Am J Otolaryngol 1994;15(2):152-4.

                                                          

   Capítulo 3.  Tumores cervicales del tejido fibroso-muscular.

  • Abraham Z, Rozenbaum M, Rosner I, Naschitz Y, Boss Y, Rosenmann E. Nuchal fibroma. J Dermatol 1997;24: 262-265. 

  • Anderson W, Kissane J. Pathology. 7ª ed. United States of America: Ed.The CV Mosby Company, 1977: 1880-1882.
  • Balakrishnan R et al. Solitary adult myofibroma of the pinna. J Laryngol Otol 1999;113(2):155-7.
  • Beck J et al. Pediatric myofibromatosis of the head and neck. Arch Otolaryngol Head Neck Surg 1999;125(1):39-44.
  • Boyd W, Anderson W. Pathology for the surgeon. 8ª ed. Ed. Sounder, 1990:83. Das Gupta TK. Tumors of the soft tissue. 1ª ed. Connecticut: Ed. Appleton Century Crofts, 1983: 412-421.
  • Coffin C, Dehner L. Fibroblastic-myofibroblastic tumors in children and adolescents: a clinic pathologic study of 108 examples in 103 patients. Pediatr Pathol 1991;11(4):569-88.
  • Chung E, Enzinger F. Infantile myofibromatosis. Cancer1981;48:1807.Das S, Upton J, Amar A. Nodular fascitis of the bladder. J Urol 1988;140: 1532-1534.
  • Duffy M, Harris M, Hornblass A. Infantile myofibromatosis of orbital bone. A case report with computed tomography, magnetic resonance imaging, and histologic findings. Ophthalmology 1997;104(9):1471-4.
  • Enzinger F, Weiss S. Soft Tissue Tumors, 4th Ed. St Louis: Mosby 2001Eze N et al. Solitary infantile myofibroma compromising the airway. International Journal of Pediatric Otorhinolaryngology 2004;68:1533-7.
  • Franzese C et al. Infantile myofibromatosis: unusual diagnosis in an older child. International Journal of Pediatric Otorhinolaryngology 2005;69(6):865-8.
  • Gangopadhyay K et al. Solitary fibrous tumor of the parapharyngeal space: a case report and review of the literature. Ear Nose Throat J 1996;75(10):681-4.
  • Hasegawa T et al. Solitary infantile myofibromatosis of bone. An immunohistochemical and ultrastructural study. Am J Surg Pathol 1993;17:308-13.
  • Hatzidaki et al. Infantile myofibromatosis with visceral involvement and complete spontaneous regression. J Dermatol 2001;28:379-82.
  • Hayry P et al. The desmoid tumor. Analysis of factors possibly contributing to the etiology and growth behavior. Am J Clin Pathol 1982;77:681-5.
  • Herrmann B et al. Lipofibromatosis presenting as a pediatric neck mass. International Journal of Pediatric Otorhinolaryngology 2004;68:1545-9.
  • Kawashima A, Goldman S, Fishman E, et al. CT of intra-abdominal desmoid tumors: Is the tumor different in patients with Gardner´s disease?. AJR 1994;162:339-342.

  • López R, Kemalyan N, Moseley H, Dennis D, Vetto R. Problems in diagnosis and management of desmoid tumors. Am J of Surg 1990; 159: 450-453.

  • Lynch H, Fitzgibbons R, Chong S, et al. Use of doxorubicin and dacarbazine for the management of unresectable intra-abdominal desmoid tumors in Gardner´s Syndrome. Dis Colon Rectum 1994;37:260-267.

  • Matthews T, Farawell V. Estadística Médica: Aplicación e interpretación. 2ª ed. Barcelona: Salvat Editores SA, 1990:71-91.

  • Michal M, Chlumska A, Povysilova V. Intranodal “amianthoid” myofibroblastoma. Report of six cases immunohistochemical and electron microscopical study. Pathol Res Pract 1992;188(1-2):199-204.

  • Montgomery E, Speight P, Fisher C. Myofibromas presenting in the oral cavity: a series of 9 cases. Oral Surg, Oral Med, Oral Pathol, Oral Radiol Endod 2000;89(3):343-8.

  • Patel SR, Evans HL, Benjamín RS. Combination chemotherapy in adult desmoid tumors. Cancer 1993;72:3244-3247.

  • Plukker J, Oort Y, Vermey A, et al. Aggressive fibromatosis (non-familial desmoid tumour): therapeutic problems and the role of adjuvant radiotherapy. Brit J of Surg 1995;82:510-514.

  • Posner M, Shui M, Newsome J, Hajdu S, Gynor J, Brennan M. The desmoid tumor. Arch Surg 1989; 124: 191-196.

  • Robbins SL, Cotran RS. Patología estructural y funcional. 3ª ed. México: Ed. Interamericana SA, 1987:1287-1288.

  • Rodríguez-Bigas M, Mahone M, Karakousis C, Petrelli N. Desmoid tumors in patients with familial adenomatous polyposis. Cancer 1994;74:1270-1274.

  • Rubin E, Farber JL. Patología 1ª ed. México: Ed. Médica Panamericana, 1990:1250.

  • Sato J et al. Solitary fibrous tumor of the parotid gland extending to the parapharyngeal space. Eur Arch Otorhinolaryngol 1998;255(1):18-21.

  • Shiu M, Weinstein L, Hajdu S, Brennan M. Malignant soft-tissue tumors of the anterior abdominal wall. The Am J of Surg 1989; 158: 446-451.

  • Siegel N, Bradford C. Fibromatosis of the Head and Neck: a challenging lesion. Otolaryngol Head Neck Surg 2000;123:269-75.

  • Sieter K, Kemeny N. Successful treatment of a desmoid tumor with doxorubicin. Cancer 1993;71:2242-2244.

  • Stautz C. Magnetic resonance evaluation of infantile myofibromatosis. Mo Med 1990;87(12):889-91.

  • Stewart R et al. Iodine-131 metaiodobenzylguanidine uptake in infantile myofibromatosis. Clin Nucl Med 1989;14(5):344-6.

  • Sweis IE, McHenry ChR, Jordan RB. Limb and life threatening desmoid tumor of the neck. Plastic and Reconstructive Surgery 1993; 92: 335-339.

  • Thomsen J, Koltai P. Sternomastoid tumor of infancy. Ann Otol Rhinol Laryngol 1989;98(12 Pt 1): 955-9.

  • Weber B et al. Diagnosis and therapy of aggressive fibromatosis (extra-abdominal desmoid) in the head and neck area. Laryngorhinootologie 1991;70(7):367-74.

  • Welling R, Hermann M, Kasper G. Experience with desmoid tumor in a Community Teaching Hospital. Journal of Surgery Oncology 1992;49:113-115.

  • Wiswell T et al: Infantile myofibromatosis: The most common fibrous tumor of infancy. J Pediatr Surg 1988;23:314.

  • Zaharia M, Moscol A, Misad O, Cáceres E, Barriga O. Valor de la radioterapia en el tratamiento de la fibromatosis agresiva. Acta Cancerológica (Perú) 1992;22:11-14.

                                                                                     

   Capítulo 4 y 5.  Paragangliomas cervicales.

  • Amar L, Bertherat J, Baudin E, Ajzenberg C, Bressac de Paiilerets B, Chabre O, Chamontin B, Delemmer B. Genetic testing in pheochromocytoma or functional paraganglioma. J Clin Oncol 2005;23:8812–8818.
  • Argiris A, Mellott A, Spies S. PET Scan Assessment of chemotherapy. Response in Metastatic Paraganglioma. Am J Clin Oncol 2003;26(6):563-66.
  • Baysal BE, Farr JE, Rubinstein WS, Galus RA, Johnson KA, Aston CE, Myers EN, Johnson JT, Carrau R, Kirkpatrick SJ, Myssiorek D, Singh D, Saha S, Gollin SM, Evans GA, James MR, Richard CW 3rd Fine mapping of an imprinted gene for familial nonchromaYn paragangliomas, on chromosome 11q23. Am J Hum Genet 1997;60:121–132.
  • Baysal BE, Willett-Brozick JE, Lawrence EC, Drovdlic CM, Savul SA, McLeod DR, Yee HA, Brackmann DE, Slattery WH 3rd, Myers EN, Ferrell RE, Rubinstein WS. Prevalence of SDHB, SDHC, and SDHD germline mutations in clinic patients with head and neck paragangliomas. J Med Genet 2002;39:178–183.
  • Benn DE, Robinson BG. Genetic basis of phaeochromocytoma and paraganglioma. Best Pract Res Clin Endocrinol Metab  2006;20:435–450.
  • Farr HW. Carotid body tumors: a thirty year experience at Memorial Hospital. Am J Surg 1967;114:614-19.
  • Favier J, Briere JJ, Strompf L, Amar L, Filali M, Jeunemaitre X, Rustin P, Gimenez-Roqueplo AP. Hereditary paraganglioma/pheochromocytoma and inherited succinate dehydrogenase deWciency. Horm Res 2005;63:171–179.
  • Hegarty JL, Lalwani AK. Paraganglioma of the head and neck: implications of molecular genetics in clinical medicine. Current Opinion in Otolaryngology Head and Neck Surgery 2003;8(5):384-90.
  • Hossam Thabet M, Hesham Kotob. Cervical paragangliomas: diagnosis, management and complications. the Journal of Laryngology & otology 2001;115:467-474.
  • Jimenez C, Cote G, Arnold A, Gagel RF. Review: should patients with apparently sporadic pheochromocytomas or paragangliomas be screened for hereditary syndromes? J Clin Endocrinol Metab 2006;91:2851–2858.
  • Kau R, Arnold W. Somatostatin receptor scintigraphy and therapy of neroendocrine (APUD) tumors or the head and neck. Acta Otolaryngol (Stockh) 1996;116:345-349.
  • Kauffmann H. Neurally mediated syncope and syncope due to autonomic failure: diferences and similarities. Journal of Clinical Neurophysiology 1997;14(3):183-96.
  • Laquis S , Valerie V , Barret H, Fleming J, Wilson M. Intracranial paraganglioma (glomus tumor) with orbital extension. Ophthalmic Plastic and Reconstructive Surgery 2001;17(6):458-61.
  • Lee JH, Barich F, Hynds Karnell L, Robinson RA, Zhen WK, Gantz BJ, Hofman HT. national Cancer Data Base Report on Malingnant paragangliomas of the Head and Neck. Cancer, 2002;94:730-737.
  • Lee SC, Chionh SB, Chong SM, Taschner PE (2003) Hereditary paraganglioma due to the SDHD M1I mutation in a second Chinesefamily: a founder eVect? Laryngoscope 2003;113:1055–1058.
  • Leonetti JP, Donzelli JJ, Littooy F, Farrell BP. Perioperative strategies in the management of carotid body tumors. Otolaryngol Head and Neck Surg 1997;117(1):111-5.
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   Capítulos 6. Tumores cervicales benignos vasculares y nerviosos.

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