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1.
Acta Chir Belg ; 113(5): 364-6, 2013.
Article in English | MEDLINE | ID: mdl-24294803

ABSTRACT

Granular cell tumors (GCT's) are uncommon soft tissue neoplasms most likely of neural or neuroectodermal origin. They can be found in virtually any body site, but they are rarely located in the abdominal wall. We report the case of a patient with a history of breast cancer presenting with a slow-growing, firm and painless nodule in the abdominal wall. After ruling out metastatic origin of the mass by CT scan and MRI, an incisional biopsy was performed. Anatomopathologic findings were congruent with a benign granular cell tumor of the abdominal wall. En-bloc surgical resection with reconstruction of the abdominal wall defect using a prosthetic mesh was performed. Preoperative histopathologic diagnosis of an abdominal wall tumor is important. Broad surgical excision to obtain negative margins should be the therapeutic goal in all cases of GCT as positive margins are highly correlated with recurrence of the lesion.


Subject(s)
Abdominal Neoplasms/surgery , Abdominal Wall , Granular Cell Tumor/surgery , Neoplasms, Second Primary/surgery , Abdominal Neoplasms/diagnostic imaging , Abdominal Neoplasms/pathology , Aged , Breast Neoplasms/epidemiology , Diagnosis, Differential , Female , Fibromatosis, Aggressive/pathology , Granular Cell Tumor/diagnostic imaging , Granular Cell Tumor/pathology , Humans , Tomography, X-Ray Computed
2.
Acta Chir Belg ; 112(5): 390-2, 2012.
Article in English | MEDLINE | ID: mdl-23175931

ABSTRACT

Gallstone ileus is a rare complication of cholelithiasis. Only 0,3-0,5% of all patients with gallstones will eventually suffer from this condition. It is well known that there is an increased prevalence of gallstones among patients with Crohn's disease, but gallstone ileus remains even in these patients an unfrequent condition. Because of the rarity of this disease and its presentation as an intestinal (sub)obstruction, mostly without biliary symptoms, diagnosis and surgical treatment are often delayed. We report the case of a 75-year-old woman with a long history of Crohn's disease presenting with intermittent symptoms of intestinal obstruction since several weeks. Symptoms were thought to be due to recurrence of Crohn's disease, but the patient did not respond to steroid therapy. Resection of the diseased ileocolic segment was performed and a large impacted stone was detected proximal of the stenotic segment. With this case report we want to emphasize how easily diagnosis of gallstone ileus can be missed, especially in Crohn's patients and we would like to discuss the different treatment options.


Subject(s)
Crohn Disease/complications , Gallstones/complications , Ileus/etiology , Aged , Female , Gallstones/diagnosis , Humans , Ileum/diagnostic imaging , Ileum/surgery , Ileus/surgery , Tomography, X-Ray Computed
3.
Acta Chir Belg ; 112(4): 314-6, 2012.
Article in English | MEDLINE | ID: mdl-23008999

ABSTRACT

Solitary fibrous tumours (SFT) of the pleura are uncommon and are incidental findings or discovered in patients with non-specific respiratory symptoms. We report a case of a 74 year old man diagnosed with a mesenchymal pleural neoplasm, associated with typical hypertrophic osteoarthropathy, referred to as Pierre-Marie-Bamberg syndrome. As reported in the literature, complete surgical resection is the gold standard for treatment of such lesions and recurrences. Radiotherapy and chemotherapy are of limited value in the curative treatment of pleural SFT. In our case surgical excision of the mass was performed. After a disease-free period of 3 years a second intervention was necessary because of recurrence. Until now our patient is free of complaints and no signs of reappearance were noted. Based on our experience and on literature findings we would like to underline the importance of regular long-term follow-up because of the substantial risk of recurrence.


Subject(s)
Solitary Fibrous Tumor, Pleural/surgery , Aged , Humans , Male , Neoplasm Recurrence, Local/surgery , Osteoarthropathy, Primary Hypertrophic/complications , Solitary Fibrous Tumor, Pleural/complications , Solitary Fibrous Tumor, Pleural/diagnostic imaging , Tomography, X-Ray Computed
4.
Acta Chir Belg ; 109(2): 224-7, 2009.
Article in English | MEDLINE | ID: mdl-19499685

ABSTRACT

Carotid artery dissection is an important cause of stroke in patients under forty years of age. A dissection of the common carotid artery is relatively rare. This condition can easily be overlooked because symptoms may be lacking or may seem trivial. Carotid artery dissection occurs mostly in previously healthy patients. Urgent treatment however, by means of coumarines or antiplatelet agents, is of life-saving importance, because this disease can lead to permanent neurological deficits or even death. We report a case of a 36-year-old patient who was admitted to the intensive care unit with hemi-paralysis and acute abdomen after a period of severe vomiting. A perforated bulbar ulcer was visible on abdominal CT scan. The patient underwent laparoscopic repair of the perforation. CT scan of the brain showed an extensive area of infarction at the region of the left medial cerebral artery. The cause of the infarction was revealed by angio CT of the supra-aortic arteries, showing a floating thrombus and a possible dissection of the left common carotid artery. Under Clopidogrel therapy, the right-sided paralysis partially recovered. Ten days post-admission, an endarterectomy of the left carotid artery was successfully performed. The patient recovered well and was discharged from the ICU 28 days after admission.


Subject(s)
Carotid Artery Thrombosis/diagnosis , Carotid Artery Thrombosis/therapy , Carotid Artery, Internal, Dissection/diagnosis , Carotid Artery, Internal, Dissection/therapy , Adult , Carotid Artery Thrombosis/etiology , Carotid Artery, Internal, Dissection/etiology , Endarterectomy, Carotid , Humans , Male , Platelet Aggregation Inhibitors/therapeutic use
5.
Acta Chir Belg ; 107(4): 402-4, 2007.
Article in English | MEDLINE | ID: mdl-17966533

ABSTRACT

Spontaneous rupture of the oesophagus (Boerhaave's syndrome) is a rare life-threatening disease requiring urgent surgical management. Symptoms can masquerade many other clinical disorders like acute myocardial infarction, dissecting aneurysm or upper gastro-intestinal tract diseases. Without prompt diagnosis and treatment, Boerhaave's syndrome has a very high mortality rate. We report a case of perforation of the distal oesophagus. A 40-year-old male patient presented at the emergency department with a classic history of acute epigastric pain and dyspnoea after an episode of vomiting. On clinical examination we found a firm, tender abdomen and cervical subcutaneous emphysema. Boerhaave's syndrome was suspected on a clinical basis and was confirmed by thoraco-abdominal CT scan, showing an apparent pneumomediastinum and fluid at both lung bases. The patient underwent surgical repair of the distal oesophageal tear by laparoscopy. A mediastinal drain was left behind and a feeding gastrostomy was established. After initial improvement, the patient developed fever and dyspnoea. A thoracic CT scan revealed left-sided empyema. A thoracoscopic drainage of pus was performed and antibacterial and antifungal treatment was adapted. The patient recovered well and was discharged from the hospital 34 days after admission.


Subject(s)
Esophageal Diseases/surgery , Laparoscopy/methods , Acute Disease , Adult , Humans , Male , Rupture, Spontaneous/surgery , Syndrome
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