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1.
Ann Fr Anesth Reanim ; 33(12): 669-76, 2014 Dec.
Article in French | MEDLINE | ID: mdl-25447779

ABSTRACT

Systemic sclerosis (SSc) is an auto-immune disease characterized by vasculopathy and the combination of microangiopathy and tissue collagen deposit leading to skin, digestive, pulmonary, myocardial and renal injuries. These repercussions could be challenging for anesthesiologists and associated with difficulties in airway management, and occurrence of congestive right heart failure or acute kidney crisis. The aim of this review is to review the physiopathology and the progression of the SSc, as well as to provide a strategy of perioperative management of these patients.


Subject(s)
Scleroderma, Systemic/surgery , Humans , Perioperative Care , Postoperative Complications/therapy
2.
Rev Neurol (Paris) ; 160(11): 1078-80, 2004 Nov.
Article in French | MEDLINE | ID: mdl-15602351

ABSTRACT

INTRODUCTION: The consequences of lightning injuries on the peripheral nervous system are widely unknown. CASE REPORT: We report on a 31 year-old woman who developed a bilateral brachial plexopathy 15 days after a lightning strike. The patient recovered progressively. CONCLUSION: Peripheral neuropathies due to lightning strikes are probably unrecognized in most of the cases, because occurrence may be delayed and only few patients were adequately investigated. Pathophysiological hypotheses are unclear and lean on experimental studies using electrical current.


Subject(s)
Brachial Plexus Neuropathies/etiology , Lightning Injuries/complications , Adult , Female , Humans
3.
Acta Endocrinol (Copenh) ; 100(2): 189-95, 1982 Jun.
Article in English | MEDLINE | ID: mdl-7113590

ABSTRACT

A large pituitary prolactinoma was found in a mentally deficient 45 year old woman presenting with amenorrhoea, galactorrhoea, headache, anaemia and hypertension, and removed surgically. She was subsequently found to have multiple adrenal aldosterone-producing adenomas, a gastric schwannoma and colonic polyadenomas. All these tumors were also removed surgically. Despite the absence of parathyroid and islet-cell hyperplasia, this case seems to be a variant of multiple endocrine neoplasia (MEN) type I.


Subject(s)
Adrenal Gland Neoplasms/metabolism , Colonic Neoplasms/metabolism , Neoplasms, Multiple Primary/metabolism , Pituitary Neoplasms/metabolism , Stomach Neoplasms/metabolism , Adenoma/metabolism , Aldosterone/metabolism , Female , Humans , Middle Aged , Neoplasms, Multiple Primary/pathology , Neurilemmoma/metabolism , Prolactin/metabolism , Syndrome
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