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1.
Rev Med Interne ; 34(1): 12-6, 2013 Jan.
Article in French | MEDLINE | ID: mdl-22884286

ABSTRACT

PURPOSE: The occurrence of acute pancreatitis in systemic lupus erythematosus (SLE) is known but rare, and is exceptionally the presenting manifestation. Its pathogenesis is multifactorial, and it is difficult to separate what belongs to vasculitis, thrombotic phenomena in the context of an associated antiphospholipid syndrome, or iatrogenic complications. We report on six cases of lupus pancreatitis. METHODS: This is a retrospective monocenter study of 110 patients with SLE. The diagnosis of lupus pancreatitis was established after exclusion of other causes of pancreatitis. RESULTS: Five women and one man (5.4%) with a mean age of 36.3 years presented with lupus pancreatitis. In four patients the pancreatitis was concurrent with the diagnosis of SLE and it occurred later during an exacerbation of the disease in the two remaining patients. In all patients, pancreatic manifestations were associated with other organ involvement. Clinical manifestations were: abdominal pain (n=6), vomiting (n=3), and fever (n=3). Elevated pancreatic enzyme was noted in all cases. All patients were treated by high doses of glucocorticoids. The outcome was favorable in five patients, and one patient died. CONCLUSION: Pancreatitis may be the presenting manifestation of SLE. Its pathogenesis is often multifactorial. The outcome is usually favorable with corticosteroids.


Subject(s)
Lupus Erythematosus, Systemic/complications , Pancreatitis/etiology , Abdominal Pain/etiology , Adult , Amylases/blood , Antibodies, Antinuclear/blood , Antibodies, Antiphospholipid/blood , Cohort Studies , Diagnosis, Differential , Female , Fever/etiology , Follow-Up Studies , Glucocorticoids/therapeutic use , Humans , Immunologic Factors/blood , Lipase/blood , Lupus Erythematosus, Systemic/diagnosis , Male , Middle Aged , Pancreatitis/diagnosis , Retrospective Studies , Ribonucleoproteins, Small Nuclear/blood , Treatment Outcome , Vomiting/etiology , Young Adult , snRNP Core Proteins/blood
2.
Rev Pneumol Clin ; 68(5): 311-4, 2012 Oct.
Article in French | MEDLINE | ID: mdl-22749953

ABSTRACT

Pulmonary artery aneurysm in Behcet disease compromises seriously the diagnosis since its fatal rupture is still the major cause of death in this disease. Pulmonary artery aneurysm requires urgent management and several treatments have been proposed, including steroids, immunosuppressive drugs, embolisation and surgery. Herein, we report a patient with Behçet's disease in whom multiple pulmonary artery aneurysms were completely resolved after a combined treatment with corticosteroids and azathioprine. Pulmonary artery aneurysms in Behçet's disease are reported to indicate poor prognosis and high mortality. Computed tomographic scans of the chest and angiography are the most common diagnostic procedures used in the diagnosis or evaluation of pulmonary artery aneurysm. Immunosuppression is the main therapy for the treatment of a vasculitis.


Subject(s)
Adrenal Cortex Hormones/administration & dosage , Aneurysm/drug therapy , Azathioprine/administration & dosage , Behcet Syndrome/drug therapy , Pulmonary Artery , Adult , Aneurysm/etiology , Behcet Syndrome/complications , Behcet Syndrome/diagnostic imaging , Drug Combinations , Humans , Immunosuppressive Agents/administration & dosage , Male , Pulmonary Artery/diagnostic imaging , Radiography, Thoracic , Remission Induction
3.
Rev Pneumol Clin ; 68(3): 194-8, 2012 Jun.
Article in French | MEDLINE | ID: mdl-22197156

ABSTRACT

Amyloidosis limited to bronchopulmonary apparatus is expressed as tracheobronchial deposits in diffuse plaques that can cause stenosis or parenchymal nodules or masses. In this regard, we report four cases of pulmonary amyloidosis and discuss the diagnostic difficulties of this location. These are two women and two men aged 60, 68, 44 and 57 years. They presented a pulmonary parenchymal amyloidosis in all cases associated with bronchial in one case. The diagnosis was confirmed by histology in all cases. The staging was negative in all cases. The evolution was marked by the stabilization of the lesions in all cases. Localized amyloidosis, which may be the only telltale sign of a systemic illness, its diagnosis requires finding other locations to better tailor the treatment strategy.


Subject(s)
Amyloidosis/diagnosis , Lung Diseases/diagnosis , Lung/pathology , Adult , Aged , Female , Humans , Lung/diagnostic imaging , Male , Middle Aged , Plaque, Amyloid/diagnosis , Radiography
4.
Rev Med Interne ; 31(4): 262-7, 2010 Apr.
Article in French | MEDLINE | ID: mdl-20170990

ABSTRACT

INTRODUCTION: Sarcoidosis is a granulomatous disorder of unknown cause, characterised by noncaseating granulomas affecting multiple organs. Gastrointestinal tract involvement in sarcoidosis is rare. The stomach, particularly the antrum is the most common extra-hepatic organ to be involved. We report four cases of gastro-intestinal sarcoidosis. METHODS: Retrospective study of a series of four cases. RESULTS: All patients had gastric sarcoidosis. It involved the duodenum, ileum and gall bladder in a patient with a history of an acute pancreatitis probably due to sarcoidosis. This patient presented with obstructive intestinal manifestations, weight loss and exsudative enteropathy. Two patients presented with mild abdominal pain and the last patient was admitted for upper gastrointestinal bleeding. The endoscopy was normal in one case and showed an antral congestion in another case. Gastric ulcers were found in the patient with a history of upper gastro-intestinal bleeding. A pseudo-linitic aspect was noticed in the patient with obstructive manifestations. The duodenum and the ileum were normal. This patient had an antrectomy and was treated with corticosteroids. Surgery evidenced a perforated duodenal ulcer, which was obstructed by the gall bladder. The patient with gastrointestinal bleeding received proton pump inhibitor and corticosteroids. These two patients improved gradually. The two other patients recovered spontaneously. CONCLUSION: The stomach is the most commonly affected organ in gastrointestinal sarcoidosis. Gastric sarcoidosis can mimic a malignant lesion owing to narrowing of the gastric lumen or can be revealed by upper gastrointestinal bleeding. Duodenum, small bowel and colon involvement is uncommon but may be underestimated in the absence of systematic biopsies.


Subject(s)
Gastrointestinal Diseases , Sarcoidosis , Adult , Female , Gastrointestinal Diseases/diagnosis , Gastrointestinal Diseases/therapy , Humans , Male , Middle Aged , Retrospective Studies , Sarcoidosis/diagnosis , Sarcoidosis/therapy
6.
Gynecol Obstet Fertil ; 33(10): 783-90, 2005 Oct.
Article in French | MEDLINE | ID: mdl-16139552

ABSTRACT

The role of exogenous estrogen in the initiation and maintenance of human systemic lupus erythematosus (SLE) remains very controversial. To review the current literature of the safety of using exogenous estrogens in patients with SLE, a Medline search for articles published between 1970 et 2004 regarding this relationship was performed. Although cohort studies suggest an increase in the incidence of SLE with both oral contraceptives and hormone replacement therapy, recent retrospective studies suggest that the risk of flares is not increased with hormone replacement therapy. Large prospective double blind placebo controlled studies inclusive of all ethnic groups such as the Safety of Estrogen in Lupus Erythematosus National Assessment (SELENA) trial had to provide the basis for definitive recommendations but it had been interrupted after WHI study results.


Subject(s)
Contraceptives, Oral, Hormonal/therapeutic use , Estrogen Replacement Therapy , Estrogens/therapeutic use , Lupus Erythematosus, Systemic/drug therapy , Contraceptives, Oral, Hormonal/adverse effects , Estrogen Replacement Therapy/adverse effects , Estrogens/adverse effects , Female , Humans , Lupus Erythematosus, Systemic/chemically induced , Safety
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