2020, Número 5
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Acta Pediatr Mex 2020; 41 (5)
Hiperplasia nodular linfoide de colon en niños: ¿un hallazgo normal o una condición patológica subestimada?
Cadena-León JF, Sempértegui-Cárdenas PX, Ignorosa-Arellano KR, Toro-Monjaráz EM, Zárate-Mondragón FE, Cervantes-Bustamante R, Ramírez-Mayans JA
Idioma: Español
Referencias bibliográficas: 55
Paginas: 215-221
Archivo PDF: 216.68 Kb.
RESUMEN
La hiperplasia nodular linfoide es la coexistencia de más de 10 nódulos linfoides protruidos hacia la luz que se advierten durante un estudio de endoscopia, por mucho
tiempo se consideró “normal” en niños; sin embargo, ahora se reporta en pacientes con
dolor abdominal crónico, constipación resistente, anemia inexplicable, sangrado de
tubo digestivo, diarrea crónica y retardo del crecimiento. Cada vez se dispone de más
evidencia que la asocia con infecciones: giardiasis, oxiuriasis, colitis por ameba o E.
coli; inmunodeficiencias: común variable, deficiencia de IgA, hipogammaglobulinemia,
VIH; alergia alimentaria; enfermedad inflamatoria intestinal y síndrome de intestino
irritable, entre otras. La confirmación se establece con el estudio histopatológico, con
hiperplasia de folículos linfoides, centros germinales con actividad mitótica y mantos
de linfocitos debidamente definidos localizados en la lámina propia o submucosa
superficial.
El tratamiento está dirigido a la causa de base, aunque no siempre es posible establecer se ha reportado la indicación de dietas de eliminación (alergia alimentaria) y
salicilatos. El potencial de malignización no está completamente demostrado; en casos
seleccionados se ha propuesto el seguimiento estrecho con estudios de endoscopia.
Es importante que el profesional de la salud conozca los hallazgos endoscópicos e
histológicos orientadores de hiperplasia nodular linfoide, los síntomas gastrointestinales
más comúnmente asociados, las causas en las que puede manifestarse y el potencial
de malignización descrito para ofrecer un mejor diagnóstico y tratamiento dirigido al
paciente pediátrico. El objetivo de esta revisión es aportar información actual referente a su definición, epidemiología, etiología, manifestaciones clínicas, diagnóstico y
tratamiento.
REFERENCIAS (EN ESTE ARTÍCULO)
Troncone R, Discepolo V. Colon in food allergy. J Pediatr Gastroenterol Nutr. 2009; 48(2):89-91. doi. 10.1097/ MPG.0b013e3181a15d1a
Kuper C. Histopathology of mucosa associated lymphoid tissue. 2006; 34: 609-615. doi. 10.1080/01926230600867735
Kunisawa J, et al. Mucosa-associated lymphoid tissues in the aerodigestive tract: their shared and divergent traits and their importance to the orchestration of the mucosal immune system. Curr Mol Med. 2005; 5:557-572. doi. 10.2174/1566524054863924
Gurkan O, et al. Colonic lymphoid nodular hyperplasia in childhood: causes of familial Mediterranean fever need extra attention. J Pediatr Gastroenterol Nutr. 2013; 57: 817-21.
Mansueto P, et al. Review article: intestinal lymphoid nodular hyperplasia in children – the relationship to food hypersensitivity. Aliment Pharmacol Ther. 2012; 35: 1000-9. doi: 10.1111/j.1365-2036.2012.05062.x.
Zahmatkeshan M, et al. Etiology of lower gastrointestinal bleeding in children: a single center experience from southern Iran. Middle East J Dig Dis. 2012; 4 (4): 216-23.
Tătăranu E, et al. Clinical, immunological and pathological profile of infants suffering from cow’s milk protein allergy. Rom J Morphol Embryol 2016; 57 (3): 1031-5.
Albuquerque A. Nodular lymphoid hyperplasia in the gastrointestinal tract colon in adults: is it common? 1990; 36: 421-422. doi. 10.1016/s0016-5107(90)71092-9
Silverio C, et al. Diagnósticos colonoscópicos más frecuentes en pediatría. Rev Cubana Pediatr. 2001; 73 (1): 28-33.
Sempértegui P, et al. Validez diagnóstica de hallazgos colonoscópicos en hiperplasia nodular linfoide en niños. Revista de Gastroenterología de México 2019; 84 (Supl 2): 62-3.
Iacono G, et al. Colonic lymphoid nodular hyperplasia in children: relationship to food hypersensitivity. Clin Gastroenterol Hepatol. 2007; 5: 361-66. https://doi. org/10.1016/j.cgh.2006.12.010
Colon A, et al. Intestinal lymphonodular hyperplasia of childhood: patterns of presentation. J Clin Gastroenterol. 1991; 13: 163-66. doi. 10.1097/00004836-199104000-00009
Ajdukiewicz A, et al. Nodular lymphoid hyperplasia with hypogammaglobulinaemia. Gut. 1972; 13: 589-595. doi. 10.1136/gut.13.8.589
Hermans P, et al. Idiopathic late-onset immunoglobulin deficiency. Clinical observations in 50 patients. Am J Med. 1976; 61: 221-237. doi. 10.1016/0002-9343(76)90173-x
Lai Ping SA, Mayer L. Gastrointestinal manifestations of primary immunodeficiency disorders. Semin Gastrointest Dis. 1997; 8: 22-32.
Bästlein C, et al. Common variable immunodeficiency syndrome and nodular lymphoid hyperplasia in the small intestine. Endoscopy. 1988; 20: 272-75. doi. 10.1055/s2007-1018192
Postgate A, et al. An unusual cause of diarrhea: diffuse intestinal nodular lymphoid hyperplasia in association with selective immunoglobulin A deficiency. Gastrointest Endosc. 2009; 70: 168-79. doi. 10.1016/j.gie.2009.03.004
Joo M, et al. Nodular lymphoid hyperplasia and histologic changes mimicking celiac disease, collagenous sprue, and lymphocytic colitis in a patient with selective IgA deficiency. Pathol Res Pract. 2009; 205: 876-80. doi. 10.1016/j.prp.2009.02.005
Webster A, et al. Nodular lymphoid hyperplasia of the bowel in primary hypogammaglobulinaemia: study of in vivo and in vitro lymphocyte function. Gut. 1977; 18: 364- 72. doi. 10.1136/gut.18.5.364
Levendoglu H, Rosen Y. Nodular lymphoid hyperplasia of gut in HIV infection. Am J Gastroenterol. 1992; 87: 1200-2.
Rubio A, et al. Clinical characteristics of a group of adults with nodular lymphoid hyperplasia: a single center experience. World J Gastroenterol. 2006; 12: 1945-48. doi. 10.3748/wjg.v12.i12.1945
Canto J, et al. Nodular lymphoid hyperplasia of the intestine. Clinic-pathologic characteristics in 11 cases. Rev Invest Clin. 1990; 42: 198-203.
Olmez S, et al. Diffuse nodular lymphoid hyperplasia of the small bowel associated with common variable immunodeficiency and giardiasis. Wien Klin Wochenschr. 2014; 126: 294-97. doi. 10.1007/s00508-014-0525-5
Onbasi K, et al. Common variable immunodeficiency (CVID) presenting with malabsorption due to giardiasis. Turk J Gastroenterol. 2005; 16: 111-13.
Baran B, et al. Nodular lymphoid hyperplasia of duodenum caused by giardiasis. Clin Gastroenterol Hepatol. 2013; 11: A22. doi. 10.1016/j.cgh.2012.12.019.
Ward H, et al. Small intestinal nodular lymphoid hyperplasia in patients with giardiasis and normal serum immunoglobulins. Gut. 1983; 24: 120-6. doi. 10.1136/gut.24.2.120
Hermans P, et al. Dysgammaglobulinemia associated with nodular lymphoid hyperplasia of the small intestine. Am J Med. 1966; 40: 78-89. doi. 10.1016/0002-9343(66)90189-6
28. Vestergaard H, et al. Association between intussusception and tonsil disease in childhood. Epidemiology. 2008; 19: 71-74. doi. 10.1097/EDE.0b013e31815c1dd3
Coulibaly B, et al. Benign lymphoid polyposis: two diffuse cases leading to fatal intestinal ischemia in children. Pediatr Int. 2009; 51: 428-31. doi. 10.1111/j.1442- 200X.2009.02824.x
Wakefield A, et al. The significance of ileocolonic lymphoid nodular hyperplasia in children with autistic spectrum disorder. Eur J Gastroenterol Hepatol. 2005; 17: 827-36.
MacDonald T. The significance of ileocolonic lymphoid nodular hyperplasia in children with autistic spectrum disorder. Eur J Gastroenterol Hepatol. 2006; 18: 569-71.
Jass J. The intestinal lesion of autistic spectrum disorder. Eur J Gastroenterol Hepatol. 2005; 1: 821-22.
Schwart D, et al. Diffuse nodular lymphoid hyperplasia of the colon: polyposis syndrome or normal variant? Gastrointest Endosc. 2003; 58: 630-32. doi. 10.1067/ S0016-5107(03)01969-2
Smith M, Blackstone M. Colonic lymphoid nodules: another cause of the red ring sign. Gastrointest Endosc. 1991; 37: 206-8. doi. 10.1016/S0016-5107(91)70692-5
Straub R, et al. Variable endoscopic appearance of colonic lymphoid tissue. J Clin Gastroenterol. 1994; 19: 158-64. doi. 10.1097/00004836-199409000-00018
Molaei M, et al. Nodular lymphoid hyperplasia in common variable immunodeficiency syndrome mimicking familial adenomatous polyposis on endoscopy. Indian J Pathol Microbiol. 2009; 52: 530-33. doi. 10.4103/0377-4929.56152
Bayraktar Y, et al. The findings of capsule endoscopy in patients with common variable immunodeficiency syndrome. Hepatogastroenterlogy. 2007; 54: 1034-37.
Shiff A, et al. Nodular lymphoid hyperplasia in a defunctionalized colon. Gastrointest Endosc. 1973; 19: 144-45. doi. 10.1016/s0016-5107(73)73985-7
Leonidas J, et al. Roentgen appearance of the excluded colon after colostomy for infantile Hirschsprung’s disease. Am J Roentgenol Radium Ther Nucl Med. 1971; 112: 116-22.
Rambaud J, et al. Diffuse follicular lymphoid hyperplasia of the small intestine without primary immunoglobulin deficiency. Am J Med. 1982; 73 (1): 125-32. doi. 10.1016/0002- 9343(82)90938-x
Washington K, et al. Gastrointestinal pathology in patients with common variable immunodeficiency and X-linked agammaglobulinemia. Am J Surg Pathol. 1996; 20: 1240-52. doi. 10.1097/00000478-199610000-00010
Albuquerque A. Nodular lymphoid hyperplasia in the gastrointestinal tract in adult patients: A review. World J Gastrointest Endosc 2014; 6 (11): 534-40 doi. 10.4253/ wjge.v6.i11.534
Bharadhwaj G, Triadafilopoulos G. Endoscopic appearances of colonic lymphoid nodules: new faces of an old histopathological entity. Am J Gastroenterol. 1995; 90: 946-950.
Laufer I, deSA D. Lymphoid follicular pattern: a normal feature of the pediatric colon. American Journal of Roentgenology. 1978; 130: 51-55. doi. 10.2214/ajr.130.1.51
Tomita S, et al. Diffuse nodular lymphoid hyperplasia of the large bowel without hypogammaglobulinemia or malabsorption syndrome: a case report and literature review. Int J Surg Pathol. 2002; 10: 297-302. doi. 10.1177/106689690201000411
Ranchod M, et al. Lymphoid hyperplasia of the gastrointestinal tract. A study of 26 cases and review of the literature. Am J Surg Pathol. 1978; 2: 383-400. doi: 10.1097/00000478-197812000-00005
Luzi G, et al. Duodenal pathology and clinicalimmunological implications in common variable immunodeficiency patients. Am J Gastroenterol. 2003; 98: 118-21. doi: 10.1111/j.1572-0241.2003.07159.x
Ament M, Rubin C. Relation of giardiasis to abnormal intestinal structure and function in gastrointestinal immunodeficiency syndromes. Gastroenterology. 1972; 62: 216-26.
Chiaramonte C, Glick S. Nodular lymphoid hyperplasia of the small bowel complicated by jejunal lymphoma in a patient with common variable immune deficiency syndrome. AJR Am J Roentgenol. 1994; 163: 1118-19. doi: 10.2214/ ajr.163.5.7976886
Ryan J. Premalignant conditions of the small intestine. Semin Gastrointest Dis. 1996; 7: 88-93.
51. Schaefer P, Friedman A. Nodular lymphoid hyperplasia of the small intestine with Burkitt’s lymphoma and dysgammaglobulinemia. Gastrointest Radiol. 1981; 6: 325-328. doi.10.1007/BF01890278.
Monsanto P, et al. Intestinal nodular lymphoid hyperplasia and extraintestinal lymphoma a rare association. Acta Gastroenterol Belg. 2012; 75: 260-62.
Jonsson O, et al. Resolution of nodular lymphoid hyperplasia of the gastrointestinal tract following chemotherapy for extraintestinal lymphoma. Dig Dis Sci. 2002; 47: 2463-65. doi. 10.1023/a:1020547723325
Rubio C. Nonprotruding colorectal neoplasms: epidemiologic viewpoint. World J Surg. 2000; 24: 1098-1105. doi. 10.1007/s002680010147
Lucarelli S, et al. Intestinal lymphoid nodular hyperplasia in children: the relationship to food allergy. Pediatr Allergy Immunol. 2015; 26 (1): 18-24. doi 10.1111/pai.12328.