ABSTRACT
Mokuboito is usually used for the treatment of patients with dyspnea and edema due to chronic heart failure. We herein report two cases successfully treated with mokuboito on the basis of shinkahiken (epigastric stuffiness and strong resistance). Case 1 was a 28-year-old woman. She had been experiencing occasional bouts of epigastralgia for 12 years, but they had worsened two months before the first visit to our department. When she was examined, however, the cause of epigastralgia could not be determined and she was diagnosed with functional gastroenteropathy. After being introduced to our department, she was treated with various Kampo formulas, but the symptom was poorly improved. Case 2 was a 74-year-old man who was prescribed hachimijiogan and shoseiryuto for an overactive bladder and perennial allergic rhinitis. His symptoms were stable, but suddenly deteriorated after two months. In both cases, when changing treatment to mokuboito on the basis of shinkahiken, the symptoms were improved. These results suggest that mokuboito can be used in a wide range of cases with shinkahiken.
ABSTRACT
A 36-year-old man underwent direct closure of an atrial septal defect through median sternotomy at the age of 14. He also underwent a mitral valve replacement with tricuspid annuloplasty using the same approach at the age of 18. The patient also presented with pretibial edema and congestive liver disease at the age of 27 and the pretibial edema progressed at the age of 35. Hypoalbuminemia (TP ; 3.6 g/dl, Alb ; 1.6 g/dl) was also observed. Further examinations were performed, which revealed that the right ventricular pressure curve presented a dip and plateau pattern by cardiac catheterization. Computed tomography of the chest additionally revealed thickened and calcified pericardium in the left ventricle. Abdominal scintigraphy showed tracer accumulation in the transverse colon hepatic flexure 4 h after intravenous administration of technetium-99m-labelled human serum albumin. The patient was diagnosed with a protein-losing gastroenteropathy caused by constrictive pericarditis. He underwent pericardiectomy via left anterior thoracotomy without cardiopulmonary bypass. No complications were present after the surgery, and he was discharged after 46 postoperative days. Following his discharge from the hospital, the pretibial edema disappeared, and serum albumin levels gradually increased and normalized within 3 months after the surgery (TP 7.1 g/dl, Alb 4.2 g/dl).
ABSTRACT
Resumen Se presentan 2 casos de enfermedad de Ménétrier (EM) remitidos a nuestra institución por síndrome edematoso. Esta enfermedad de poca prevalencia es una gastropatía hipertrófica perdedora de proteínas que en la mayoría de los casos es de causa desconocida, aunque se ha asociado con procesos infecciosos. Se caracteriza por edema, hipoproteinemia, hipoalbuminemia y, en la infancia, es de carácter benigno y autolimitado.
Abstract We present two cases of Menétrier's Disease (MS) referred to our institution due to edema. The prevalence of this disease is low. It is a hypertrophic gastropathy which causes loss of proteins and which has unknown causes in the majority of cases although it has been associated with infectious processes. It is characterized by edema, hypoproteinemia, hypoalbuminemia. In childhood it is benign and self-limited.
Subject(s)
Humans , Male , Infant , Child, Preschool , Disease , Hypoalbuminemia , Gastritis, Hypertrophic , Hypoproteinemia , SyndromeABSTRACT
Introducción: la gastroenteropatía eosinofílica es una enfermedad rara caracterizada por infiltración de eosinófilos en una o más capas a diferentes niveles del tracto grastrointestinal, siendo común en estómago y duodeno. Aunque en la mayoría de los casos se presenta con dolor abdominal, también puede aparecer vómito, diarrea, ascitis y pérdida de peso. Reporte de caso: hombre de 41 años con cuadro clínico de 9 meses de evolución de dolor abdominal súbito e intermitente, de predominio en mesogastrio irradiado a región lumbar, manejado con antiespasmódicos sin mejoría. Antecedentes de: infarto agudo de miocardio 2 años atrás con arterias coronarias sanas según angiografía, nefrectomía derecha hace 11 años por hidronefrosis, diagnóstico y tratamiento desde hace 3 años de anemia microcítica hipocrómica con hipereosinofilia, apendicitis aguda hace 7 meses con hallazgos en la patología de infiltrados eosinofílicos, y una biopsia de médula ósea que reveló eosinofilia. Al examen físico: signos vitales normales, ruidos intestinales aumentados en intensidad y frecuencia (40/min) y mesogastrio doloroso a la palpación; sin masas ni visceromegalias. Sus laboratorios revelaron anemia y eosinofilia de 16%. Las imágenes diagnósticas reportaron una esofagogastroileítis, con evidencia microscópica de infiltración eosinofila en todas las muestras, por lo cual se diagnosticó gastroenteropatía eosinofílica iniciando manejo con dieta hipoalergénica y prednisona. Discusión: hasta 25% de los pacientes con síndrome hipereosinofílico puede tener infiltración gastrointestinal, por lo que la gastroenteropatía eosinofílica debe sospecharse en todo paciente con dolor abdominal y eosinofilia periférica, no obstante, esta última no siempre está presente, siendo necesario un diagnóstico histopatológico.
Introduction: Eosinophilic gastroenteropathy is a rare disease characterized by infiltration of eosinophils into one or more layers in different parts of the gastrointestinal tract especially the stomach and the duodenum. Although in most cases it presents with abdominal pain, vomiting, diarrhea, ascites and weight loss may also appear. Case report: The patient was a 41 year old man with a clinical picture of 9 months of sudden, intermittent abdominal pain (predominantly mesogastric pain which radiated to the lumbar region). He had been treated with antispasmodics but had not improved. Eleven years earlier he had had a right nephrectomy because of hydronephrosis. Three years earlier he had been diagnosed and treated for hypochromic microcytic anemia with hypereosinophilia. Two years earlier he had had an acute myocardial infarct, although angiography showed healthy coronary arteries. Seven months earlier he developed acute appendicitis. The pathology report at that time showed eosinophilic infiltrates, and a bone marrow biopsy revealed eosinophilia. Physical examination showed normal vital signs, but his bowel sounds were more intense and frequent (40/min) than normal, and he suffered mesogastric pain on palpation. There were no masses or organomegaly. Laboratory tests revealed anemia and 16% eosinophilia. Diagnostic images showed esophageal and gastric ileitis with microscopic evidence of eosinophil infiltration in all samples. Eosinophilic gastroenteropathy was diagnosed, and the patient was started on a hypoallergenic diet and treated with prednisone. Up to 25% of patients with hypereosinophilic syndrome may have gastrointestinal infiltration. Eosinophilic gastroenteropathy should be suspected in any patient with abdominal pain and peripheral eosinophilia. However, peripheral eosinophilia is not always present, and histopathological diagnosis is necessary.
Subject(s)
Humans , Male , Adult , Gastroenteritis , Gastrointestinal Diseases , Hypereosinophilic SyndromeABSTRACT
La enfermedad de Ménétrier infantil es una gastroenteropatía perdedora de proteínas caracterizada por hipertrofa de la mucosa gástrica, de causa desconocida, aunque la mayoría de los casos informados se han asociado a infecciones virales. Se manifesta clínicamente por edema y bioquímicamente por hipoproteinemia e hipoalbuminemia. Es poco común en los niños, en quienes tiene un carácter benigno y autolimitado, a diferencia de los adultos, en los que tiende a cronifcarse y, en ocasiones, a malignizarse. Se presenta un caso de enfermedad de Ménétrier infantil con síndrome ascítico edematoso posiblemente asociado a una infección por citomegalovirus.
Ménétrier's disease is a childhood protein-losing gastroenteropathy characterized by hypertrophy of the gastric mucosa, of unknown etiology, although most of reported cases have been associated with viral infections. Clinical manifestation is edema and biochemically there are hypoproteinemia and hypoalbuminemia. This disease is very rare in children and they have a benign and self-limiting course in contrast to adults where tend to be chronic and occasionally to become malignant. We present a child with Ménétrier disease with edema and ascites possibly associated with a cytomegalovirus infection.
Subject(s)
Child, Preschool , Humans , Male , Cytomegalovirus Infections/complications , Gastritis, Hypertrophic/virology , Protein-Losing Enteropathies/virologyABSTRACT
Ye Gui was praised in medical faculty for his knowledge and experience of nourishing fluid in stomach,however after reading his medical record all over,Ye Gui' academic idea of diffusing and obstruction-removing gastric yang in treating gastroenteropathy based on syndrome differentiation was more outstanding.The theory was based on "no vigorous gastric yang insulted easily gathered turbid yin".The concrete application features were in terms of "obstruction-removing and tonifying yangming meridians,and together treating liver and stomach","combination of diffusing and obstruction-removing gastric yang,warming spleen and removing obstruction in collaterals et al" and so on.Adopting the method of diffusing and obstruction-removing gastric yang at the right moment especially benefited the treatment of gastroenteropathy based on syndrome differentiation.
ABSTRACT
PURPOSE: Henoch-Schonlein purpura (HSP) is a small-vessel vasculitic disease that most often affects the skin. Abdominal symptoms precede the typical purpuric rash of HSP in 14~36%. It is a challenge to diagnose HSP in the absence of a rash, because there are no biologic tests that can identify HSP with certainty, so we tried to find out the characteristic features of HSP gastroenteropathy without purpura before diagnosis. METHODS: This study included 82 children with HSP who had been admitted or visited outward of the Department of Pediatrics, Pusan National University Hospital from 1995 to 2000. The cases that the onset of purpura preceded or coincided that of abdominal pain were defined as purpura-positive group. The cases that the onset of abdominal pain preceded purpura more than 1 week and purpura was not presented till diagnosed as HSP gastroenteropathy were defined as purpura-negative group. We compared and analyzed the clinical features of the two groups by reviewing the medical records retrospectively. To ensure the diagnosis of HSP gastroenteropathy, we conducted upper GI series, abdominal ultrasonogram, abdominal CT, endoscopy and/or skin biopsy. RESULTS: The number of cases of purpura-positive group and purpura-negative group were 72 and 10, respectively. There is no difference between two groups in the incidence of clinical symptoms and laboratory findings. Children with HSP gastroenteropathy had characteristic erosive or ulcerative lesions in the stomach or duodenum on esophagogastroduodenoscopy, or mural thickening of the small bowel on abdominal ultrasonogram, CT or upper GI series. Skin biopsy revealed leukocytoclastic vasculitis in 3 of them, although biopsy specimen was taken from any areas of normal-appearing skin. In purpura-negative group, 9 patients improved by steroid therapy. CONCLUSION: In purpura-negative group, there is no diagnostic feature on the laboratory findings and clinical features. Therefore, to diagnose HSP gastroenteropathy in patients with abdominal pain in the absence of the characteristic rash, careful observation of clinical features and laboratory data, and prompt application of available diagnostic tools such as gastrointestinal endoscopy, radiologic study and skin biopsy are recommended. Early use of corticosteroid may reduce the suffering in these patients.