Jornal Vascular Brasileiro
https://app.periodikos.com.br/journal/jvb/article/doi/10.1590/1677-5449.005615
Jornal Vascular Brasileiro
Therapeutic Challenge

Desafios clínicos e psicossociais no tratamento de um paciente com síndrome de Proteus

Clinical and psychosocial challenges in the treatment of a patient with Proteus syndrome

Matheus Bertanha; Regina Moura; Marcone Lima Sobreira; Lied Martins Santiago Pereira; Rodrigo Gibin Jaldin; Manuella Pacífico de Freitas Segredo; Hamilton Almeida Rollo; Winston Bonetti Yoshida

Downloads: 1
Views: 2764

Resumo

Resumo A Síndrome de Proteus é uma rara associação de malformações que podem afetar vários tecidos e órgãos. É caracterizada por macrodactilia bilateral, hipertrofia craniana, anomalias ósseas, escoliose, hamartomas de tecidos moles, nevo verrucoso pigmentar, anormalidades viscerais e outras hipertrofias. Há pouco mais de 200 casos notificados em todo o mundo. O presente artigo relata a evolução clínica de um paciente pediátrico com essa síndrome. A criança apresentou desnutrição grave associada ao extremo gigantismo de membros inferiores. Além disso, apresentou repercussões psicossociais relacionadas à exclusão social. A doença tornou-se mais grave e progrediu como síndrome consumptiva. Finalmente, os pais concordaram com a amputação dos membros inferiores hipertróficos. Um ano após as amputações, a criança estava totalmente reabilitada, protetizada dos membros amputados, com melhora nutricional, além de apresentar notória recuperação psicológica e reinserção social, o que representou melhora significativa da qualidade de vida para o paciente.

Palavras-chave

amputação, anormalidades congênitas, anormalidades musculosqueléticas

Abstract

Abstract Proteus syndrome is a rare combination of malformations that can affect several tissues and organs. It is characterized by bilateral macrodactyly, cranial hypertrophy, bone anomalies, scoliosis, soft-tissue hamartomas, verrucous pigmented nevus, visceral abnormalities and other forms of hypertrophy. Just over 200 cases have been reported worldwide. This article reports on the clinical course of a pediatric patient with this syndrome. The child had severe malnutrition associated with extreme gigantism of the lower limbs and also psychosocial problems related to social exclusion. As the disease progressed it exacerbated and evolved into a wasting syndrome. After several years, the parents agreed to amputation of the hypertrophic lower limbs. One year after the amputations the child had been rehabilitated and had adapted to prostheses, with nutritional improvement and notable psychological recovery and social reintegration, which represented a significant improvement in his quality of life.

Keywords

amputation, congenital abnormalities, musculoskeletal abnormalities

References

Cohen Jr MM, Hayden P. A newly recognized hamartomatous syndrome. Birth Defects Orig Artic Ser. 1979;15(5B):291-6.

Wiedemann HR, Burgio GR, Aldenhoff P, Kunze J, Kaufmann HJ, Schirg E. The proteus syndrome: partial gigantism of the hands and/or feet, nevi, hemihypertrophy, subcutaneous tumors, macrocephaly or other skull anomalies and possible accelerated growth and visceral affections. Eur J Pediatr. 1983;140(1):5-12.

Sakamoto Y, Nakajima H, Kishi K, Shimizu R, Nakajima T. Management of craniofacial hyperostosis in Proteus syndrome. J Craniofac Surg. 2010;21(2):414-8.

Pazzaglia UE, Beluffi G, Bonaspetti G, Ranchetti F. Bone malformations in Proteus syndrome: an analysis of bone structural changes and their evolution during growth. Pediatr Radiol. 2007;37(8):829-35.

White NJ, Cochrane DD, Beauchamp R. Paraparesis caused by an angiolipomatous hamartoma in an adolescent with Proteus syndrome and scoliosis. J Neurosurg. 2005;103(3^sSupl):282-4.

Samlaska CP, Levin SW, James WD, Benson PM, Walker JC, Perlik PC. Proteus syndrome. Arch Dermatol. 1989;125(8):1109-14.

Barmakian JT, Posner MA, Silver L, Lehman W, Vine DT. Proteus syndrome. J Hand Surg Am. 1992;17(1):32-4.

Biesecker L. The challenges of Proteus syndrome: diagnosis and management. Eur J Hum Genet. 2006;14(11):1151-7.

Turner JT, Cohen Jr MM, Biesecker LG. Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases. Am J Med Genet A. 2004;130A(2):111-22.

Stricker S. Musculoskeletal manifestations of Proteus syndrome: report of two cases with literature review. J Pediatr Orthop. 1992;12(5):667-74.

Thomason JL, Abramowsky CR, Rickets RR, Culbertson JH, Clifton MS, Shehata BM. Proteus syndrome: three case reports with a review of the literature. Fetal Pediatr Pathol. 2012;31(3):145-53.

Gontijo B, Pereira LB, Silva CMR. Malformações vasculares. An Bras Dermatol. 2004;79(1):7-25.

Satter E. Proteus syndrome: 2 case reports and a review of the literature. Cutis. 2007;80(4):297-302.

Cohen Jr MM. Proteus syndrome: clinical evidence for somatic mosaicism and selective review. Am J Med Genet. 1993;47(5):645-52.

Lindhurst MJ, Sapp JC, Teer JK. A mosaic activating mutation in AKT1 associated with the Proteus syndrome. N Engl J Med. 2011;365(7):611-9.

Vieira NRN, Pereira LB, Silva CMR, Gontijo B. Síndrome de Proteus: relato de caso. An Bras Dermatol. 2001;76:201-8.

Raju RR, Hart WR, Magnuson DK, Reid JR, Rogers DG. Genital tract tumors in Proteus syndrome: report of a case of bilateral paraovarian endometrioid cystic tumors of borderline malignancy and review of the literature. Mod Pathol. 2002;15(2):172-80.

Kaduthodil MJ, Prasad DS, Lowe AS, Punekar AS, Yeung S, Kay CL. Imaging manifestations in Proteus syndrome: an unusual multisystem developmental disorder. Br J Radiol. 2012;85(1017):e793-9.

Li CY, Chang YL, Chen WC, Lee YC. Pulmonary manifestations and management of proteus syndrome. J Formos Med Assoc. 2010;109(5):397-400.

Abbo O, Bouali O, Galinier P, Moscovici J. Proteus syndrome: case report of bladder vascular malformation causing massive hematuria. Prog Urol. 2012;22(2):132-5.

Lublin M, Schwartzentruber DJ, Lukish J, Chester C, Biesecker LG, Newman KD. Principles for the surgical management of patients with Proteus syndrome and patients with overgrowth not meeting Proteus criteria. J Pediatr Surg. 2002;37(7):1013-20.

Adolphs N, Tinschert S, Bier J, Klein M. Craniofacial hyperostoses in Proteus syndrome: a case report. J Craniomaxillofac Surg. 2004;32(6):391-4.

Becktor KB, Becktor JP, Karnes PS, Keller EE. Craniofacial and dental manifestations of Proteus syndrome: a case report. Cleft Palate Craniofac J. 2002;39(2):233-45.

Nazario APM, Alves MR, Ellis C, Morais FC, Panico MB, Vieira GM. Síndrome de Proteus: hamartose desde o nascimento. J Vasc Bras. 2011;10:124.

Havard S, Enjolras O, Lessana-Leibowitch M, Escande JP. Proteus syndrome. 8 cases. Ann Dermatol Venereol. 1994;121(4):303-8.

Sociedade Brasileira de Angiologia e Cirurgia Vascular (SBACV)"> Sociedade Brasileira de Angiologia e Cirurgia Vascular (SBACV)">
5ddecda50e88251b407279a1 jvb Articles

J Vasc Bras

Share this page
Page Sections