Literature DB >> 9428835

Systemic capillary leak syndrome: report on 13 patients with special focus on course and treatment.

Z Amoura1, T Papo, J Ninet, P Y Hatron, J Guillaumie, A M Piette, O Blétry, P Dequiedt, A Talasczka, E Rondeau, J L Dutel, B Wechsler, J C Piette.   

Abstract

BACKGROUND: Systemic capillary leak syndrome (SCLS) is a rare condition characterized by unexplained episodic capillary hyperpermeability due to a shift of fluid and protein from the intravascular to the interstitial space. This results in diffuse swelling, weight gain, and renal shut-down. From the first publication in 1960, only 34 cases have been reported.
OBJECTIVE: To collate enough patients to observe the natural history of the disease and evaluate the efficacy of empiric treatments.
DESIGN: Multicentric retrospective study.
RESULTS: Thirteen patients (6 women and 7 men) were collated with a mean follow-up of 6.4 years. Eight patients are still alive after a mean of 5.6 years (range 1 to 15). Three patients out of the 11 who were not lost to follow-up died; 1 during an attack and 2 because of a progression towards multiple myeloma.
CONCLUSIONS: Our series shows an improvement in the prognosis of SCLS due most likely to improved management during attacks. Some patients' disease could evolve into a multiple myeloma. Treatment is still empiric and no prophylactic therapy, including terbutaline associated with aminophylline, has clearly proven its efficacy.

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Year:  1997        PMID: 9428835     DOI: 10.1016/s0002-9343(97)00272-6

Source DB:  PubMed          Journal:  Am J Med        ISSN: 0002-9343            Impact factor:   4.965


  29 in total

1.  Morphea presenting as widespread oedema.

Authors:  Hamish Dobbie; John Lanham; Robert Unwin
Journal:  J R Soc Med       Date:  2002-09       Impact factor: 5.344

Review 2.  Narrative review: the systemic capillary leak syndrome.

Authors:  Kirk M Druey; Philip R Greipp
Journal:  Ann Intern Med       Date:  2010-07-20       Impact factor: 25.391

Review 3.  [Systemic capillary leak syndrome causes a compartment syndrome of both lower legs and a forearm. A case report with a review of the literature].

Authors:  P Balcarek; K-H Frosch; M Quintel; K M Stürmer
Journal:  Unfallchirurg       Date:  2005-09       Impact factor: 1.000

4.  Monoclonal gammopathy of undetermined significance: significant beyond hematology.

Authors:  Steven Vanderschueren; Marieke Mylle; Daan Dierickx; Michel Delforge; Peter Verhamme; Kathelijne Peerlinck; Wouter Meersseman; Daniël C Knockaert
Journal:  Mayo Clin Proc       Date:  2009-09       Impact factor: 7.616

Review 5.  Idiopathic systemic capillary leak syndrome (Clarkson disease).

Authors:  Kirk M Druey; Samir M Parikh
Journal:  J Allergy Clin Immunol       Date:  2016-12-22       Impact factor: 10.793

6.  Compartment syndrome in all four extremities: a rare case associated with systemic capillary leak syndrome.

Authors:  Rodger H Brown; Cara Downey; Shayan Izaddoost
Journal:  Hand (N Y)       Date:  2010-10-26

7.  Vascular endothelial hyperpermeability induces the clinical symptoms of Clarkson disease (the systemic capillary leak syndrome).

Authors:  Zhihui Xie; Chandra C Ghosh; Roshni Patel; Shoko Iwaki; Donna Gaskins; Celeste Nelson; Nina Jones; Philip R Greipp; Samir M Parikh; Kirk M Druey
Journal:  Blood       Date:  2012-03-12       Impact factor: 22.113

8.  A case report of idiopathic systemic capillary leak syndrome that occurred during the postoperative period of abdominoperineal resection for colorectal cancer.

Authors:  Tsuyoshi Ozawa; Hironori Yamaguchi; Tomomichi Kiyomatsu; Shinsuke Saito; Soichiro Ishihara; Eiji Sunami; Joji Kitayama; Toshiaki Watanabe
Journal:  Int Surg       Date:  2015-01

9.  [A 52-year old female patient with recurrent shock of unclear origin, hemoconcentration and hypoalbuminemia].

Authors:  M Müller; A Schmidt
Journal:  Internist (Berl)       Date:  2004-05       Impact factor: 0.743

Review 10.  [Idiopathic systemic capillary leak syndrome (Clarkson disease) : A rare cause of recurrent life-threatening edema].

Authors:  S Dasdelen; S-O Grebe
Journal:  Internist (Berl)       Date:  2018-07       Impact factor: 0.743

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