Segmental necrotizing jejunitis is characterized by severe abdominal pain of acute onset, bilious vomitings and foul smelling loose stools containing blood. Pathologic features include circumferential intestinal wall inflammation ranging from edema with minimal congestion to severe congestion, hemorrhage with necrosis, ulceration, and gangrene with perforation. Early diagnosis and suitable supportive measures prevent unnecessary laparatomy and complications. There was no report of this disease entity in children in Korea. We experienced a case of segmental necrotizing jejunitis with fever, abdominal pain and bloody stools, which was diagnosed by exploration and was treated successfully by antibiotics and supportive measures.ope
Erythropoietic protoporphyria is a genetic disorder due to a deficiency of ferrochelatase resulting ...
A bronchogenic cyst is congenital malformation of the foregut which was generally encountered within...
Gitelman�셲 syndrome is a primary renal tubular disorder characterized by chronic hypokalemia, hypoma...
Isolated rectal adenomatous polyp without genetic background is rarely found in children. A 4-year a...
Laparoscopic hysterectomy is currently considered the standard procedure in many patients who need h...
Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome, a kind of hypersensitivity syndr...
The clinicopathological manifestations of gastric mucormycosis range from colonization of ulcer dise...
Subungual exostosis is a benign, acquired tumor of cartilaginous bone which occurs beneath the nail ...
Polypoid tumors of the gallbladder are diagnosed very rarely in children; there are only 13 cases of...
Noonan syndrome is featured by short stature, mental retardation, facial dysmorphia, webbed neck, an...
Congenital diaphragmatic eventration is the abnormal elevation of the diaphragm into the thoracic ca...
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Olfactory neuroblastoma is a rare, malignant neoplasm arising from the olfactory epithelium. It has ...
Primary intestinal lymphangiectasia is a congenital lymphatic disorder in which intestinal lymphatic...
BACKGROUND AND OBJECTIVES: Pectoralis major myocutaneous flap(PMMCF) is a workhorse flap of head an...
Erythropoietic protoporphyria is a genetic disorder due to a deficiency of ferrochelatase resulting ...
A bronchogenic cyst is congenital malformation of the foregut which was generally encountered within...
Gitelman�셲 syndrome is a primary renal tubular disorder characterized by chronic hypokalemia, hypoma...
Isolated rectal adenomatous polyp without genetic background is rarely found in children. A 4-year a...
Laparoscopic hysterectomy is currently considered the standard procedure in many patients who need h...
Drug rash with eosinophilia and systemic symptoms (DRESS) syndrome, a kind of hypersensitivity syndr...
The clinicopathological manifestations of gastric mucormycosis range from colonization of ulcer dise...
Subungual exostosis is a benign, acquired tumor of cartilaginous bone which occurs beneath the nail ...
Polypoid tumors of the gallbladder are diagnosed very rarely in children; there are only 13 cases of...
Noonan syndrome is featured by short stature, mental retardation, facial dysmorphia, webbed neck, an...
Congenital diaphragmatic eventration is the abnormal elevation of the diaphragm into the thoracic ca...
The physiologic changes produced by hypothermia include impairments in the stress response and immun...
Olfactory neuroblastoma is a rare, malignant neoplasm arising from the olfactory epithelium. It has ...
Primary intestinal lymphangiectasia is a congenital lymphatic disorder in which intestinal lymphatic...
BACKGROUND AND OBJECTIVES: Pectoralis major myocutaneous flap(PMMCF) is a workhorse flap of head an...
Erythropoietic protoporphyria is a genetic disorder due to a deficiency of ferrochelatase resulting ...
A bronchogenic cyst is congenital malformation of the foregut which was generally encountered within...
Gitelman�셲 syndrome is a primary renal tubular disorder characterized by chronic hypokalemia, hypoma...