Síndrome de Allgrove sin acalasia esofágica: Reporte de un caso
PDF

Palabras clave

Acalasia del esófago
Insuficiencia suprarrenal
Alacrimia
Síndrome de Allgrove
Reporte de caso Esophageal Achalasia
Adrenal Insufficiency
Lacrimal Apparatus Diseases
Allgrove Syndrome
Case report

Cómo citar

Quintero-Palacios, M. A. . ., Nofal-Ladino, J. J. ., Roa-Rodríguez, S. M. ., & Palacios-Ariza, M. A. . (2022). Síndrome de Allgrove sin acalasia esofágica: Reporte de un caso. Revista Médica Sanitas, 25(1), 7-14. https://doi.org/10.26852/01234250.612

Resumen

El síndrome de Allgrove es una enfermedad huérfana, con patrón de herencia autosómica recesiva caracterizada por insuficiencia suprarrenal, acalasia y alacrimia. Se describe el caso de un paciente masculino preescolar previamente sano, que ingresa a urgencias de una institución de 4to nivel de atención con deshidratación y mal estado general. El paciente completó 25 días hospitalizado en donde presentó múltiples paros cardiorrespiratorios, neumonía aspirativa, hipoglicemia sintomática persistente y pobre respuesta a corticoides, por lo que se sospechó una enfermedad metabólica. En consulta ambulatoria por endocrinología pediátrica llama la atención características adicionales como: hipercromía generalizada de la piel, alacrimia e inadecuada ganancia de peso y talla, sin reflujo gastroesofágico o acalasia. El síndrome de Allgrove es una patología con un amplio espectro de manifestaciones que se debe tener en cuenta a pesar de no presentarse con la triada usual.

https://doi.org/10.26852/01234250.612
PDF

Citas

Allgrove J, Clayden GS, Grant DB, Macaulay JC. Familial glucocorticoid deficiency with achalasia of the cardia and deficient tear production. Lancet. 1978 Jun 17;1(8077):1284–6. https://10.1016/s0140-6736(78)91268-0

Roucher-Boulez F, Perriere AB de la, Jacquez A, Chau D, Guignat L, Vial C, et al. Triple-A syndrome: a wide spectrum of adrenal dysfunction. European Journal of Endocrinology. 2018 Mar 1;178(3):199–207. https://10.1530/EJE-17-0642

Tullio-Pelet A, Salomon R, Hadj-Rabia S, Mugnier C, de Laet MH, Chaouachi B, et al. Mutant WD-repeat protein in triple-A syndrome. Nat Genet. 2000 Nov;26(3):332–5. https://10.1038/81642

Polat R, Ustyol A, Tuncez E, Guran T. A broad range of symptoms in allgrove syndrome: single center experience in Southeast Anatolia. J Endocrinol Invest. 2020 Feb;43(2):185–96. https://10.1007/s40618-019-01099-2

Goswami S, Roy A, Bhattacharjee R, Shivaprasad KS, Chakraborty PP, Selvan C, et al. The “Double A” phenotype: Portending Allgrove’s syndrome and averting adrenal crisis. Indian J Endocrinol Metab. 2012 Dec;16(Suppl 2):S367–8. https://10.4103/2230-8210.104095

Kasar PA, Khadilkar VV, Tibrewala VN. Allgrove syndrome. Indian J Pediatr. 2007 Oct;74(10):959–61. https://10.1007/s12098-007-0179-7

Diaz J, Kane TD, Leon E. Evidence of GMPPA founder mutation in indigenous Guatemalan population associated with alacrima, achalasia, and mental retardation syndrome. Am J Med Genet. 2020 Mar;182(3):425–30. https://10.1002/ajmg.a.61476

Koehler K, Hackmann K, Landgraf D, Schubert T, Shakiba M, Kariminejad A, et al. Homozygous deletion of the entire AAAS gene in a triple A syndrome patient. European Journal of Medical Genetics. 2019 Jul;62(7):103665. https://10.1016/j.ejmg.2019.05.004

Singh K, Puri RD, Bhai P, Arya AD, Chawla G, Saxena R, et al. Clinical heterogeneity and molecular profile of triple A syndrome: a study of seven cases. J Pediatr Endocrinol Metab. 2018 Jul 26;31(7):799–807. https://10.1515/jpem-2018-0023

Tibussek D, Ghosh S, Huebner A, Schaper J, Mayatepek E, Koehler K. “Crying without tears” as an early diagnostic sign-post of triple A (Allgrove) syndrome: two case reports. BMC Pediatr. 2018 Jan 15;18(1):6. https://10.1186/s12887-017-0973-y

Gaiani F, Gismondi P, Minelli R, Casadio G, de’Angelis N, Fornaroli F, et al. Case report of a familial triple: a syndrome and review of the literature. Medicine (Baltimore). 2020 May 29;99(22):e20474. https://https://10.1097/MD.0000000000020474

Bouliari A, Lu X, Persky RW, Stratakis CA. Triple A syndrome: two siblings with a novel mutation in the AAAS gene. Hormones (Athens). 2019 Mar;18(1):109–12. https://10.1007/s42000-018-0089-2

Ismail AF, Mohamed S, Ezz-Elregal M, Talat I, Muthurajan S, Fouda A. Associations with hypoglycemia are useful: a case report of Allgrove syndrome. Turk J Gastroenterol. 2012;23(5):608–9. https://10.4318/tjg.2012.0384

Flokas ME, Tomani M, Agdere L, Brown B. Triple A syndrome (Allgrove syndrome): improving outcomes with a multidisciplinary approach. PHMT. 2019 Aug;Volume 10:99–106. https://10.2147/JMDH.S178507

Dhar M, Verma N, Singh RB, Pai VK. Triple A to triple S: From diagnosis, to anesthetic management of Allgrove syndrome. J Clin Anesth. 2016 Sep;33:141–3. https://10.1016/j.jclinane.2016.02.035

Roman S, Nicolino M, Mion F, Tullio-Pelet A, Péré-Vergé D, Souquet JC. Triple-a syndrome: a rare etiology of adult achalasia. Dig Dis Sci. 2005 Mar;50(3):440–2. https://10.1007/s10620-005-2454-7

MaheshKumar K, Mahadevan S, Ramaswamy P. 4th A in a triple A syndrome - A rare case report. J Basic Clin Physiol Pharmacol. 2020 Jun 24;31(6). https://10.1515/jbcpp-2019-0293

Vishnu VY, Modi M, Prabhakar S, Bhansali A, Goyal MK. “A” motor neuron disease. J Neurol Sci. 2014 Jan 15;336(1–2):251–3.

Jayant SS, Gupta R, Agrawal K, Das L, Dutta P, Bhansali A. Triple A (Allgrove) syndrome due to AAAS gene mutation with a rare association of amyotrophy. Hormones (Athens). 2021 Mar;20(1):197–205. https://10.1007/s42000-020-00217-7

Manoria P. Triple A syndrome: a case report. Trop Doct. 2021 Apr;51(2):263–5. https://10.1177/0049475520961944

Li Y, Fallon SC, Helmrath MA, Gilger M, Brandt ML. Surgical treatment of infantile achalasia: a case report and literature review. Pediatr Surg Int. 2014 Jun;30(6):677–9. https://10.1007/s00383-014-3493-y

Descargas

Los datos de descargas todavía no están disponibles.