1.A Case of Spontaneous Pneumomediastinum and Pneumopericardium in a Patient with Acute Exacerbation of Idiopathic Pulmonary Fibrosis.
Se Young YUN ; Yong Ho KIM ; Eun Kyoung CHOI ; Seuk Kyun HONG ; Young Ku JI ; Kye Young LEE ; Young Hi CHOI ; Na Hye MYONG ; Jae Seuk PARK
Tuberculosis and Respiratory Diseases 2001;50(6):704-709
Background: Spontaneous pneumopericardium is a very rare condition. Spontaneous pneumothorax and pneumomediastinum have been reported to be associated with an idiopathic pulmonary fibrosis (IPF). However, spontaneous pneumopericardium has not yet been reported in association with IPF. Here we report a case of spontaneous pneumomediastinum and pneumopericardium in a patient with acute exacerbation of IPF with a review of the relevant literature.
Humans
;
Idiopathic Pulmonary Fibrosis*
;
Mediastinal Emphysema*
;
Pneumopericardium*
;
Pneumothorax
2.A Very Rare Cause of Chronic Intestinal Pseudo-Obstruction: Sopradic Visceral Myopathy.
Tae Hun KIM ; Seung Jae MYUNG ; Young Mi LEE ; Hye Sook JANG ; Hye kyoung SONG ; Jin Hyug LEE ; Hwoon Yong JUNG ; Seuk Kyun YANG ; Woon Sun HONG ; Jin Ho KIM ; Young Il MIN ; Chang Sik YU ; Jung Sun KIM
Korean Journal of Gastrointestinal Motility 2002;8(2):202-207
Chronic intestinal pseudo-obstruction syndrome (CIPS) is a rare clinical condition in which impaired intestinal propulsion causes recurrent symptoms of bowel obstruction in the absence of mechanical obstruction. CIPS can be present as either primary or secondary although the latter is rare in children compared with adults. The primary abnormality consists of a degeneration of either the muscularis propria (visceral myopathy), or the myenteric plexus (visceral neuropathy). A 19 year old woman was recently admitted with recurrent abdominal distension and diarrhea. An abdominal plain X-ray revealed a marked dilated stomach and duodenum with some air-fluid levels. A small bowel series showed a diffusely dilated small bowel with multifocal angulation and spiculation. Computed tomograpy also revealed a dilated small bowel and distal ileal wall thickening. The patient was treated by duodenojejunostomy and ileal resection. Histologically the intestine showed thinning of the proper muscle layer with degeneration of smooth muscle cells replaced by fibrosis. Based on the specific histopathologic finding, in addition to the clinical history, physical finding and radiological evaluation, a diagnosis of sporadic visceral myopathy was rendered. The patient was treated through total parenteral nutrition with neostigmine, prokinetics, octreotide, and erythromycin postoperatively. However, she underwent ileostomy due to poor response from these therapies. After ileostomy, she improved without a recurrence of severe symptoms.
Adult
;
Child
;
Diagnosis
;
Diarrhea
;
Duodenum
;
Erythromycin
;
Female
;
Fibrosis
;
Humans
;
Ileostomy
;
Intestinal Pseudo-Obstruction*
;
Intestines
;
Myenteric Plexus
;
Myocytes, Smooth Muscle
;
Neostigmine
;
Octreotide
;
Parenteral Nutrition, Total
;
Recurrence
;
Stomach
;
Young Adult
3.A Very Rare Cause of Chronic Intestinal Pseudo-Obstruction: Sopradic Visceral Myopathy.
Tae Hun KIM ; Seung Jae MYUNG ; Young Mi LEE ; Hye Sook JANG ; Hye kyoung SONG ; Jin Hyug LEE ; Hwoon Yong JUNG ; Seuk Kyun YANG ; Woon Sun HONG ; Jin Ho KIM ; Young Il MIN ; Chang Sik YU ; Jung Sun KIM
Korean Journal of Gastrointestinal Motility 2002;8(2):202-207
Chronic intestinal pseudo-obstruction syndrome (CIPS) is a rare clinical condition in which impaired intestinal propulsion causes recurrent symptoms of bowel obstruction in the absence of mechanical obstruction. CIPS can be present as either primary or secondary although the latter is rare in children compared with adults. The primary abnormality consists of a degeneration of either the muscularis propria (visceral myopathy), or the myenteric plexus (visceral neuropathy). A 19 year old woman was recently admitted with recurrent abdominal distension and diarrhea. An abdominal plain X-ray revealed a marked dilated stomach and duodenum with some air-fluid levels. A small bowel series showed a diffusely dilated small bowel with multifocal angulation and spiculation. Computed tomograpy also revealed a dilated small bowel and distal ileal wall thickening. The patient was treated by duodenojejunostomy and ileal resection. Histologically the intestine showed thinning of the proper muscle layer with degeneration of smooth muscle cells replaced by fibrosis. Based on the specific histopathologic finding, in addition to the clinical history, physical finding and radiological evaluation, a diagnosis of sporadic visceral myopathy was rendered. The patient was treated through total parenteral nutrition with neostigmine, prokinetics, octreotide, and erythromycin postoperatively. However, she underwent ileostomy due to poor response from these therapies. After ileostomy, she improved without a recurrence of severe symptoms.
Adult
;
Child
;
Diagnosis
;
Diarrhea
;
Duodenum
;
Erythromycin
;
Female
;
Fibrosis
;
Humans
;
Ileostomy
;
Intestinal Pseudo-Obstruction*
;
Intestines
;
Myenteric Plexus
;
Myocytes, Smooth Muscle
;
Neostigmine
;
Octreotide
;
Parenteral Nutrition, Total
;
Recurrence
;
Stomach
;
Young Adult