共查询到20条相似文献,搜索用时 0 毫秒
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E S Chemla A Raynaud B Mongrédien M A Combes N D'Attellis C F Cardon P L Julia J F Toussaint J N Fabiani 《Journal of vascular surgery》2001,34(4):743-747
Entrapment syndrome below or just above the elbow is uncommon. These rare causes of neurologic or vascular entrapment are linked to anomalous anatomical structures. No case of entrapment syndrome has been reported in patients with angioaccess for hemodialysis. We report, for the first time, forearm arteries entrapment in two patients presenting with recurrent angioaccess for hemodialysis thrombosis. Anatomical, radiologic, and surgical features of these uncommon syndromes are discussed. 相似文献
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Doebler RW 《Urology》2000,55(2):286
The differential diagnosis of recurrent bacteriuria includes a host of conditions very familiar to urologists. Ureterorectal fistula represents an unusual clinical entity that can cause recurrent bacteriuria. We present a patient who ultimately proved to have such a fistula. We review the available literature and comment on the significance of this condition. 相似文献
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S Aftab T Yasmeen MH Hamid M Sarwar H Sipra A Qureshi A Sheikh N Haider G Hanif 《Journal of the College of Physicians and Surgeons--Pakistan : JCPSP》2012,22(8):536-538
Pheochromocytomas are rare neuroendocrine tumours of chromaffin tissues. They are catecholamine secreting tumours which cause severe hypertension and other systemic disturbances. Of all the causes of childhood hypertension, pheochromocytoma constitutes less than 1%. We report the case of a 12 years old child who presented with hypertensive encephalopathy, confirmed histologically to be secondary to pheochromocytoma, and cured with meticulous critical care and surgical resection. 相似文献
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Khan JA Masood T Shamsi F 《Journal of the College of Physicians and Surgeons--Pakistan : JCPSP》2012,22(2):123-125
Patients with nephrotic syndrome are at risk of developing thrombosis in both veins and arteries. Various manifestations in different organs have been reported. Thrombi in heart seen, associated with multiorgan thrombosis have been reported on autopsy earlier, but only once in a living patient with nephrotic syndrome. Here, we report a 13 years old boy with steroid-resistant nephrotic syndrome, who developed an asymptomatic but potentially hazardous large intracardiac thrombus. The child developed nephrotic syndrome at the age of 9 years and had multiple recurrences. At the age of 13 years, he developed myocardial infarction (MI) due to embolism from a large intracardiac thrombus. Later on, he was treated with heparin and warfarin anticoagulation. 相似文献
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Hereditary angioedema is a rare disease, which is caused by deficiency of compleman c1 esterase inhibitor regulatory protein in the compleman system. Priapism is involuntary, painful and prolonged erection of penis more than 4 h without sexual desire. In this case report, we elucidated a patient diagnosed with hereditary angioedema while he had recurrent priapism. 相似文献
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Khan JA Panwar Z Mujtaba F Shah K 《Journal of the College of Physicians and Surgeons--Pakistan : JCPSP》2012,22(4):248-249
This is a case report of a 26 years old female who presented in emergency with sudden onset of chest heaviness and dyspnoea. She had suffered a stroke in the past and was treated with anti-tuberculous medication. Her ECG revealed STelevation myocardial infarction and thrombolysis was performed but was unsuccessful. Further workup during in-hospital stay revealed evidence of infective endocarditis and Streptococcus species were isolated. She was started on penicillin and gentamycin with good recovery. This case presented a management problem during initial presentation as there was insufficient data on thrombolysis during such situation. It is also a diagnostic problem as the initial picture was dominated by acute coronary syndrome. There is need to develop consensus based on expert opinion about management in such situations. 相似文献
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Mircelal Kazimi Murat Ulas Cem Ibis Mutlu Unver Nazan Ozsan Funda Yilmaz Galip Ersoz Murat Zeytunlu Murat Kilic Ahmet Coker 《World journal of emergency surgery : WJES》2009,4(1):1-4
We describe a case of life-threatening small bowel haemorrhage in a 56 year old man, who was found to have partial midgut
malrotation at laparotomy. An association between congenital malrotation and gastrointestinal haemorrhage has not previously
been reported in this age group. We discuss the association between gut malrotation and small intestinal pathology and describe
the principles of management in these patients. 相似文献
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Mircelal Kazimi Murat Ulas Cem Ibis Mutlu Unver Nazan Ozsan Funda Yilmaz Galip Ersoz Murat Zeytunlu Murat Kilic Ahmet Coker 《World journal of emergency surgery : WJES》2009,4(1):5
Lower gastrointestinal hemorrhage accounts for approximately 20% of gastrointestinal hemorrhage. The most common causes of
lower gastrointestinal hemorrhage in adults are diverticular disease, inflammatory bowel disease, benign anorectal diseases,
intestinal neoplasias, coagulopathies and arterio-venous malformations. Hemangiomas of gastrointestinal tract are rare. Mesenteric
hemangiomas are also extremely rare. 相似文献
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Tuberculosis affecting the rectum is a rare extra‐pulmonary form of the disease that needs recognition, because it requires specific treatment and avoids multiple, unwarranted surgical interventions. The following discussion is centred on a case of rectal tuberculosis, a disease that rarely affects the anorectal region. The condition was diagnosed on histology and was successfully treated medically with complete resolution. 相似文献
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Morini F Quattrucci S Cozzi DA Tancredi G Cicconi AM Guidi R Midulla F 《The Annals of thoracic surgery》2003,76(6):2085-2087
Primary lung tumors are rare in childhood and often overlooked owing to the nonspecific presentation. We report the case of a 15-year-old boy with a 3-year history of recurrent pneumonia always involving the right lower lobe due to bronchial mucinous adenoma. After endoscopic removal the tumor recurred locally, necessitating open surgical resection of the tumor. In a child with localized recurrent pneumonia of uncertain pathogenesis, the differential diagnosis should include a primary lung tumor. Bronchial adenomas should not be removed endoscopically; patients must undergo open thoracotomy for surgical excision. 相似文献
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Diverticulosis of the main bronchi: a rare cause of recurrent bronchopneumonia in a child.
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Diverticulosis of the main bronchi, not associated with other organ abnormalities, developed in a 12 year old child. This abnormality caused recurrent bronchopneumonia in the lung with the main bronchi diverticulosis. Fibreoptic bronchoscopy helped to locate the lesion and selective bronchography, with injection of contrast medium through the suction channel of the fibreoptic bronchoscope, showed the morphology of this rare malformation. 相似文献
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Masayuki Chida Muneo Minowa Syunsuke Eba Hajime Odajima 《General thoracic and cardiovascular surgery》2009,57(3):166-168
A 14-year-old girl had a left spontaneous pneumothorax. Because closed chest tube drainage failed to obtain expansion of the
lung, thoracoscopic bullectomy was performed. Pathological examination of the bulla resulted in the diagnosis of mesenchymal
cystic hamartoma, which is a rare cause of pneumothorax. 相似文献
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