RESUMEN
Pseudopolyps, a type of remnant oxyntic mucosa on a background of corpus-restricted mucosal atrophy, are a characteristic endoscopic finding in autoimmune gastritis (AIG). Linear or nodular enterochromaffin-like (ECL) cell hyperplasia, a characteristic histopathological finding of AIG, is not generally found in pseudopolyps. We report a case of AIG with fundic gland polyp (FGP)-like pseudopolyps containing nodular ECL cell hyperplasia. A 64-year-old man underwent esophagogastroduodenoscopy, which revealed atrophic changes limited to the corpus, with a normal antrum. The greater curvature was less atrophic than the lesser curvature. Sessile or semipedunculated polypoid lesions were observed on the greater curvature and on the anterior and posterior walls of the corpus. The polypoid lesions resembled FGPs, although some were larger than FGPs generally are. Histologically, non-atrophic fundic glands with parietal cell pseudohypertrophy were observed in the upper regions of the polypoid lesions. By contrast, at the base of the lesions, where linear and nodular ECL cell hyperplasia was identified by immunohistochemical staining, destruction of fundic glands with lymphocytic infiltration, loss of parietal cells, and pseudopyloric metaplasia was observed. Anti-parietal cell antibody positivity and hypergastrinemia confirmed the diagnosis of AIG with pseudopolyps. FGP-like pseudopolyps can, therefore, be present with nodular ECL cell hyperplasia in AIG.
Asunto(s)
Células Similares a las Enterocromafines , Gastritis Atrófica , Gastritis , Neoplasias Gástricas , Células Similares a las Enterocromafines/patología , Mucosa Gástrica/patología , Gastritis/diagnóstico , Gastritis Atrófica/diagnóstico , Gastritis Atrófica/patología , Humanos , Hiperplasia/patología , Masculino , Persona de Mediana Edad , Neoplasias Gástricas/patologíaRESUMEN
We herein report two cases of autoimmune gastritis without complete atrophy of the corpus. Both were positive for anti-parietal cell antibodies. Endoscopic examinations indicated that atrophic changes were predominant in the lesser curvature of the corpus in both cases. In one, the greater curvature was covered with pseudopolyp-like nodules, whereas the greater curvature of the other showed multiple similar nodules and mildly atrophic mucosa. Histopathological examinations of these nodules showed focal and patchy atrophy and preserved fundic glands with parietal cell pseudohypertrophy. Follow-up endoscopy and a repeated biopsy demonstrated the development of gastric atrophy on the greater curvature in both cases.
Asunto(s)
Atrofia/diagnóstico por imagen , Enfermedades Autoinmunes/diagnóstico , Enfermedades Autoinmunes/fisiopatología , Gastritis Atrófica/diagnóstico , Gastritis Atrófica/fisiopatología , Hipertrofia/diagnóstico por imagen , Pólipos/diagnóstico por imagen , Anciano , Autoanticuerpos , Biopsia , Diagnóstico Precoz , Femenino , Humanos , Japón , Masculino , Persona de Mediana Edad , Resultado del TratamientoAsunto(s)
Adenocarcinoma/diagnóstico , Pólipos del Colon/diagnóstico , Neoplasias del Colon Sigmoide/diagnóstico , Adenocarcinoma/patología , Adenocarcinoma/terapia , Adulto , Protocolos de Quimioterapia Combinada Antineoplásica/uso terapéutico , Quimioterapia Adyuvante/métodos , Colectomía , Colon Sigmoide/diagnóstico por imagen , Colon Sigmoide/patología , Colon Sigmoide/cirugía , Pólipos del Colon/patología , Pólipos del Colon/cirugía , Colonoscopía , Femenino , Fluorouracilo/uso terapéutico , Humanos , Leucovorina/uso terapéutico , Compuestos Organoplatinos/uso terapéutico , Neoplasias del Colon Sigmoide/patología , Neoplasias del Colon Sigmoide/terapiaRESUMEN
Urinary schistosomiasis is a tropical infection with a high endemicity in the developing countries and is included in the list of "Neglected Tropical Diseases". It is caused by a parasitic worm, Schistosoma haematobium, and it has come into the spotlight as a major cause of urogenital disease. Furthermore, it is linked to bladder cancer and it is a predisposing factor for HIV/AIDS. In this case, we describe a bladder schistosomal disease in a young African boy with persistent macroscopic hematuria and its ultrasound diagnostic bladder imaging.