1.Asymptomatic Pneumatosis Intestinalis in Immune-competent Adult.
The Korean Journal of Gastroenterology 2012;59(2):197-199
No abstract available.
Adult
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Colonoscopy
;
Humans
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Male
;
Pneumatosis Cystoides Intestinalis/*diagnosis
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Tomography, X-Ray Computed
2.Pneumatosis Cystoides Intestinalis With Portal Venous Gas: Two Case Reports.
Jong O KIM ; Kyung Hwan KIM ; Dae Kon SOHN ; Ah Jin KIM ; Tae Kyung KIM
Journal of the Korean Society of Emergency Medicine 2004;15(1):47-50
Pneumatosis cystoides intestinalis is a rare condition which is characterized by multiple gas-filled cysts of varying sizes in the wall of the gastrointestinal tract. In 85% of the cases, it is associated with gastrointestinal, pulmonary, and connective tissue diseases or with other conditions. In about 15% of the cases, the etiology remains obscure. In most cases, the prognosis is poor, so early diagnosis and treatment are required. We report two cases of primary pneumatosis cystoides intestinalis with portal venous gas which were associated with alcoholism and diabetes mellites and which were complicated by pneumoperitoneum and panperitonitis.
Alcoholism
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Connective Tissue Diseases
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Early Diagnosis
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Gastrointestinal Tract
;
Pneumatosis Cystoides Intestinalis*
;
Pneumoperitoneum
;
Portal Vein
;
Prognosis
3.Pneumatosis Intestinalis with Pneumoperitoneum Mimicking Intestinal Perforation in a Patient with Myelodysplastic Syndrome after Hematopoietic Stem Cell Transplantation.
Bhumsuk KEAM ; Jeong Hoon LEE ; Myoung Don OH ; Inho KIM ; Sung Soo YOON ; Byoung Kook KIM ; Seonyang PARK
The Korean Journal of Internal Medicine 2007;22(1):40-44
Pneumatosis intestinalis (PI) is an uncommon disorder characterized by an accumulation of gas in the bowel wall, and has been associated with a variety of disorders and procedures. We describe a 35-year-old man who undertook hematopoietic stem cell transplantation due to myelodysplastic syndrome. An abdominal X-ray demonstrated extensive PI with pneumoperitoneum mimicking hollow organ perforation. However, the patient had no abdominal symptoms and there was no evidence of peritoneal inflammation. After two weeks of conservative management, including bowel rest and antibiotics, his pneumoperitoneum resolved spontaneously without any complications. Of the many factors that affect the gastrointestinal tract mucosal integrity, intramural pressure, and bacterial flora-produced intraluminal gas interact to produce PI. If the condition is accompanied by bowel ischemia, portomesenteric venous gas, metabolic acidosis, and abdominal sepsis, or if PI is severe in extent immediate surgical intervention is indicated. The described case supports that a mechanical rather than a bacterial etiology underlies the pathogenesis of PI.
Pneumoperitoneum/*diagnosis
;
Pneumatosis Cystoides Intestinalis/*diagnosis/pathology/therapy
;
Myelodysplastic Syndromes/*diagnosis/pathology
;
Male
;
Intestinal Perforation/*diagnosis
;
Humans
;
*Hematopoietic Stem Cell Transplantation
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Diagnosis, Differential
;
Adult
4.A Case of Necrotizing Colitis Presenting with Hepatic Portal Venous Gas and Pneumatosis Intestinalis.
Jong Gyu SONG ; Ja Seol KOO ; Hyo Sung KANG ; Jin Yong PARK ; Seoung Young KIM ; Jong Jin HYUN ; Sung Woo JUNG ; Sang Woo LEE
The Korean Journal of Gastroenterology 2015;65(3):177-181
Hepatic portal venous gas is a very rare radiologic sign which is characterized by gas accumulation in the portal venous circulation. Pneumatosis intestinalis is also very rare and is characterized by multiple air cysts in the serosal or submucosal layers of the gastrointestinal tract walls. These two findings are caused by various pathological conditions and can develop individually or simultaneously. The latter is clinically more significant because it is frequently related to bowel ischemia or necrosis, and represents a poor prognosis. However, prognosis is more influenced by the severity of underlying disease rather than hepatic portal venous gas or pneumatosis intestinalis itself. If bowel ischemia or necrosis is the primary cause, emergency operation is very important to improve patient's prognosis. Herein, we report a case of necrotizing colitis presenting as hepatic portal venous gas and pneumatosis intestinalis which was successfully managed by early surgery.
Colitis/complications/*diagnosis/surgery
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Humans
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Intestinal Perforation
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Male
;
Middle Aged
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Necrosis
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Pneumatosis Cystoides Intestinalis/complications/*diagnosis
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Portal Vein
;
Radiography, Abdominal
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Tomography, X-Ray Computed
5.A Case of Recurrent Pneumatosis Cystoides Intestinalis Associated with Recurrent Pneumoperitoneum.
Ju Yee PARK ; Jae Young YOON ; Sun Yang MIN ; Seung Kwon HONG ; Ju Sang PARK ; Eun Jeong JANG ; Hyun Wook BAIK ; Sang Jong PARK
The Korean Journal of Gastroenterology 2007;50(3):188-192
Pneumatosis cystoides intestinalis is an uncommon condition of unknown etiology, characterized by the presence of multiple gas filled cysts in the gastrointestinal tract. Many different causes of pneumatosis cystoides intestinalis have been proposed, including mechanical, pulmonary, and bacterial causes. Approximately 85% of cases are thought to be secondary to coexisting disorders of the gastrointestinal tract or the respiratory system. The condition has been associated with the therapeutic uses of lactulose, steroids, and various cancer chemotherapeutic regimens. Lactitol is a disaccharide analogue of lactulose which is available as a pure crystalline powder. There are three previous case reports suggestive of lactulose causing pnumatosis intestinalis. We report a case of recurrent pneumatosis cystoides intestinalis associated with benign recurrent pneumoperitoneum developed probably secondary to lactitol therapy.
Adult
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Cathartics/adverse effects/therapeutic use
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Female
;
Humans
;
Pneumatosis Cystoides Intestinalis/*diagnosis/etiology/radiography
;
Pneumoperitoneum/complications/*diagnosis
;
Recurrence
;
Sugar Alcohols/adverse effects/therapeutic use
;
Tomography, X-Ray Computed
7.A Case of Pneumatosis Cystoides Intestinalis.
In Hae PARK ; Jae Hee CHO ; Chang Hwan CHOI ; Sang Kil LEE ; Tae Il KIM ; Ho Guen KIM ; Won Ho KIM
Korean Journal of Gastrointestinal Endoscopy 2005;30(6):336-339
Pneumatosis cystoides intestinalis (PCI) is a rare condition defined as the presence of multiple gas-filled cysts in the wall of gastrointestinal tract. The etiology and pathogenesis of PCI remain uncertain. It is associated with various medicosurgical conditions, including various pulmonary and gastointestinal diseases, connective tissue diseases and endoscopic procedures. The diagnosis is confirmed by endoscopic puncture and biopsy. PCI in adults, for the most part, show a benign clinical course and better prognosis if the associated disease is well controlled. Infantile PCI is more serious condition and especially associated with necrotizing enteritis. The treatment is usually conservative, However surgical intervention is needed when complications such as intussusception, obstruction, bleeding and perforation develope. We experienced a case of PCI found during the follow-up colonoscopy in a patient taken right hemicolectomy and systemic adjuvant chemotherapy due to colon cancer.
Adult
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Biopsy
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Chemotherapy, Adjuvant
;
Colonic Neoplasms
;
Colonoscopy
;
Connective Tissue Diseases
;
Diagnosis
;
Drug Therapy
;
Enteritis
;
Follow-Up Studies
;
Gastrointestinal Tract
;
Hemorrhage
;
Humans
;
Intussusception
;
Pneumatosis Cystoides Intestinalis*
;
Prognosis
;
Punctures
8.Pneumatosis Cystoides Intestinales and Portomesenteric Venous Gas following Anticholinesterase Pesticide Poisoning.
Suk Hee LEE ; Kyung Woo LEE ; Jin Hee JUNG
Journal of The Korean Society of Clinical Toxicology 2017;15(1):56-59
Pneumatosis cystoides intestinalis and portomesenteric venous gas are uncommon radiological findings, but are found commonly in cases of bowel ischemia, or as a result of various non-ischemic conditions. A 72-year-old man visited an emergency center with altered mental status 2 hours after ingestion of an unknown pesticide. On physical examination, he showed the characteristic hydrocarbon or garlic-like odor, miotic pupils with no response to light, rhinorrhea, shallow respiration, bronchorrhea, and sweating over his face, chest and abdomen. Laboratory results revealed decreased serum cholinesterase, as well as elevated amylase and lipase level. We made the clinical diagnosis of organophosphate poisoning in this patient based on the clinical features, duration of symptoms and signs, and level of serum cholinesterase. Activated charcoal, fluid, and antidotes were administered after gastric lavage. A computerized tomography scan of the abdomen with intravenous contrast showed acute pancreatitis, poor enhancement of the small bowel, pneumatosis cystoides intestinalis, portomesenteric venous gas and ascites. Emergent laparotomy could not be performed because of his poor physical condition and refusal of treatment by his family. The possible mechanisms were believed to be direct intestinal mucosal damage by pancreatic enzymes and secondary mucosal disruption due to bowel ischemia caused by shock and the use of inotropics. Physicians should be warned about the possibility of pneumatosis cystoides intestinalis and portomesenteric venous gas as a complication of pancreatitis following anticholinesterase poisoning.
Abdomen
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Aged
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Amylases
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Antidotes
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Ascites
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Charcoal
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Cholinesterases
;
Diagnosis
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Eating
;
Emergencies
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Gastric Lavage
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Humans
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Ischemia
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Laparotomy
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Lipase
;
Odors
;
Organophosphate Poisoning
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Pancreatitis
;
Physical Examination
;
Pneumatosis Cystoides Intestinalis
;
Poisoning*
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Pupil
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Respiration
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Shock
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Sweat
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Sweating
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Thorax
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Treatment Refusal
9.A Case of Pneumatosis Intestinalis Associated with Sunitinib Treatment for Renal Cell Carcinoma.
Yoo A CHOI ; Eun Hui SIM ; Kyoung Eun LEE ; Sun Young KO ; Min Ji SEO ; Young Jun YANG ; Ji Chan PARK ; Suk Young PARK
The Korean Journal of Gastroenterology 2013;61(6):347-350
Sunitinib as a multitarget tyrosine kinase inhibitor is one of the anti-tumor agents, approved by the United States Food and Drug Administration to use treat gastrointestinal stromal tumor and metastatic renal cell carcinoma. The agent is known to commonly induce adverse reactions such as fatigue, nausea, diarrhea, stomatitis, esophagitis, hypertension, skin toxicity, reduciton in cardiac output of left ventricle, and hypothyroidism. However, it has been reported to rarely induce adverse reactions such as nephrotic syndrome and irreversible reduction in renal functions, and cases of intestinal perforation or pneumatosis interstinalis as such reactions have been consistently reported. In this report, a 66-year old man showing abdominal pain had renal cell carcinoma and history of sunitinib at a dosage of 50 mg/day on a 4-weeks-on, 2-weeks-off schedule. Seven days after the third cycle he was referred to the hospital because of abdominal pain. Computed tomography showed pneumoperitoneum with linear pneumatosis intestinalis in his small bowel. The patient underwent surgical exploration that confirmed the pneumatosis intestinalis at 100 cm distal to Treitz's ligament. We report a rare case of intestinal perforation with pneumatosis intestinalis after administration of sunitinib to a patient with metastatic renal cell carcinoma.
Aged
;
Antineoplastic Agents/adverse effects/*therapeutic use
;
Carcinoma, Renal Cell/*drug therapy
;
Drug Administration Schedule
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Humans
;
Indoles/adverse effects/*therapeutic use
;
Intestinal Perforation/*diagnosis/etiology/surgery
;
Kidney Neoplasms/*drug therapy
;
Lung/radiography
;
Male
;
Pneumatosis Cystoides Intestinalis/*diagnosis/etiology
;
Positron-Emission Tomography
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Pyrroles/adverse effects/*therapeutic use
;
Tomography, X-Ray Computed
10.A Case of Pneumatosis Cystoids Intestinalis with Polymyositis.
Soon Jae LEE ; Ji Young PARK ; Se Ah KWON ; Dong Hee KOH ; Min Ho CHOI ; Hyun Ju JANG ; Sea Hyub KAE ; Jin LEE
The Korean Journal of Gastroenterology 2011;57(4):249-252
Pneumatosis cystoides intestinalis (PCI), characterized by presence of intramural gas cyst in the intestinal wall is associated with various medical condition. Polymyosistis, however, is rarely associated with PCI. Few cases are reported in the world, and none has not been reported previously in Korea. A 67-year-old woman with polymyositis developed mild abdominal pain and abdominal distension during treatment with steroid and azathioprine. Radiographic findings including CT scan showed intraperitoneal free gas and intramural air, compatible with PCI. The patient's symptom and clinical findings improved after the treatment with antibiotics and high-dose oxygen therapy.
Aged
;
Anti-Bacterial Agents/therapeutic use
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Anti-Inflammatory Agents/therapeutic use
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Azathioprine/therapeutic use
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Cefotaxime/therapeutic use
;
Female
;
Humans
;
Oxygen Inhalation Therapy
;
Pneumatosis Cystoides Intestinalis/complications/*diagnosis/drug therapy
;
Polymyositis/complications/*diagnosis/drug therapy
;
Prednisolone/therapeutic use
;
Radiography, Abdominal
;
Tomography, X-Ray Computed