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Panniculitis

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701. A pilot study of thalidomide for patients with symptomatic mesenteric panniculitis. (PubMed)

A pilot study of thalidomide for patients with symptomatic mesenteric panniculitis. Mesenteric panniculitis is a rare condition with no standard therapy.To assess the safety and efficacy of thalidomide for the treatment of patients with symptomatic mesenteric panniculitis using a newly established clinical disease activity index (Mesenteric Panniculitis Subjective Assessment Score).In an open-label pilot study, five patients with symptomatic mesenteric panniculitis received oral thalidomide (...) , 200 mg nightly, for 12 weeks. The primary end-point was a reduction in the Mesenteric Panniculitis Subjective Assessment Score by > or = 20% at 12 weeks or complete remission (absence of symptoms).Four (80%) of the five patients responded. The median Mesenteric Panniculitis Subjective Assessment Score at baseline was 39 and at week 12 was 25 (average decrease of 44%). One patient achieved complete remission by week 4, which was sustained. At 12 weeks, three (75%) patients experienced a global

2002 Alimentary Pharmacology & Therapeutics

702. Panniculitis-like T-cell lymphoma clinically manifested as alopecia. (PubMed)

Panniculitis-like T-cell lymphoma clinically manifested as alopecia. A 45-year-old women presented with multifocal scalp lesions with the clinical impression of alopecia areata. Histological findings first suggested cytophagic histiocytic panniculitis, although a 'burned-out' panniculitis-like T-cell lymphoma could not be excluded. After a 20-month follow-up period, assessment of the T-cell receptor gamma-chain gene rearrangement verified the diagnosis of subcutaneous panniculitis-like T-cell

2002 British Journal of Dermatology

703. Severe panniculitis caused by homozygous ZZ alpha1-antitrypsin deficiency treated successfully with human purified enzyme (Prolastin). (PubMed)

Severe panniculitis caused by homozygous ZZ alpha1-antitrypsin deficiency treated successfully with human purified enzyme (Prolastin). Severe panniculitis caused by alpha1-antitrypsin deficiency is very rare even though the ZZ phenotype occurs in 1 : 3500 of the population of northern Europe. We describe a 33-year-old woman with rapidly progressing panniculitis and extensive skin necrosis with multiple life-threatening complications. Initial treatment followed by maintenance therapy with human

2002 British Journal of Dermatology

704. Pyogranulomatous panniculitis in a cat associated with infection by the Mycobacterium fortuitum/peregrinum group (PubMed)

Pyogranulomatous panniculitis in a cat associated with infection by the Mycobacterium fortuitum/peregrinum group A 6-year-old, spayed female, American domestic shorthair was presented with a 10-month history of nodules on the dorsum. Diagnosis of pyogranulomatous panniculitis caused by Mycobacterium fortuitum/peregrinum group was achieved by using tissue culture, chromatography, and histopathologic examination. Pathological findings, diagnosis, and clinical management of the condition

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2002 The Canadian Veterinary Journal

705. Lobular panniculitis associated with ciprofloxacin. (PubMed)

Lobular panniculitis associated with ciprofloxacin. 2379015 1990 09 13 2018 11 13 0959-8138 300 6737 1990 Jun 02 BMJ (Clinical research ed.) BMJ Lobular panniculitis associated with ciprofloxacin. 1468 Rodríguez E E Hospital de L'Esperit Sant, Barcelona, Spain. Martínez J A JA Torres M M Nubiola A A Buges J J eng Case Reports Journal Article England BMJ 8900488 0959-8138 5E8K9I0O4U Ciprofloxacin AIM IM Aged Ciprofloxacin adverse effects Female Humans Panniculitis chemically induced 1990 6 2

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1990 BMJ : British Medical Journal

706. Treatment with cimetidine of atypical fasciitis panniculitis syndrome. (PubMed)

Treatment with cimetidine of atypical fasciitis panniculitis syndrome. Three patients presented with septal fasciitis and panniculitis, associated with clinical and laboratory features which precluded straight-forward classification into eosinophilic fasciitis, localised scleroderma, or lupus erythematosus profundus. Treatment with cimetidine caused the remission of cutaneous manifestations and the extracutaneous abnormalities, such as nailfold capillary disturbances and the presence (...) of antithyroid antibodies, improved. It is concluded that features of eosinophilic fasciitis or localised scleroderma and certain additional atypical elements should be categorised as atypical fasciitis-panniculitis syndrome.

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1990 Annals of the Rheumatic Diseases

707. Nodular Panniculitis in a Female Toy Poodle (PubMed)

Nodular Panniculitis in a Female Toy Poodle A four month old female toy Poodle showing multiple nodules 2 to 3 cm in diameter, some of which had ruptured over the neck and trunk area, was diagnosed as having nodular panniculitis. The animal had been treated with a course of chloramphenicol and ampicillin for one month with no response. The diagnosis was based on history, clinical signs, laboratory data and dramatic response to the addition of corticosteroid to the antibiotic therapy.

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1983 The Canadian Veterinary Journal

708. Panniculitis: a report of four cases and literature review. (PubMed)

Panniculitis: a report of four cases and literature review. Panniculitis is a disease with many causes and associations. The classification of clinical subtypes is unsatisfactory and hampered by the use of eponyms. Four children with recurring panniculitis are described and their histology presented. Three had subcutaneous fat atrophy with lobular panniculitis on biopsy; all responded well to corticosteroids. The fourth child had a septal panniculitis with no atrophy of subcutaneous tissues (...) and only a partial response to treatment with corticosteroids. A widely accepted precise histological classification of panniculitis is needed to enable accurate predictions of the outcome of this serious disorder.

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1991 Archives of Disease in Childhood

709. Granulomatous lipophagic panniculitis and temporal arteritis in a patient with cryptogenic chronic active hepatitis. (PubMed)

Granulomatous lipophagic panniculitis and temporal arteritis in a patient with cryptogenic chronic active hepatitis. An elderly woman receiving long term treatment with prednisone and azathioprine for cryptogenic chronic active hepatitis developed granulomatous lipophagic panniculitis and temporal arteritis. The lymphoplasmahistiocytic inflammatory reaction pattern is common to this patient's three diseases. It is suggested that an aberration of the defence mechanisms, immunological (...) or otherwise, is responsible for this unusual occurrence. The triple association of chronic active hepatitis, granulomatous panniculitis and temporal arteritis has not been reported previously.

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1992 Annals of the Rheumatic Diseases

710. Weber-Christian panniculitis. (PubMed)

Weber-Christian panniculitis. Two cases of Weber-Christian panniculitis with onset at 7 months and 3 years 6 months are described. Both show evidence of disturbances in immune mechanisms. The family of the first case has a high prevalence of coeliac disease, and the mother of the first patient also suffers from alopecia areata and dermatitis herpetiformis.

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1987 Annals of the Rheumatic Diseases

711. Mesenteric panniculitis. (PubMed)

Mesenteric panniculitis. 3176478 1988 10 28 2018 11 13 0093-0415 148 6 1988 Jun The Western journal of medicine West. J. Med. Mesenteric panniculitis. 700-1 Khachaturian T T Hughes J J eng Case Reports Journal Article United States West J Med 0410504 0093-0415 AIM IM Aged Aged, 80 and over Humans Male Mesentery pathology Panniculitis, Nodular Nonsuppurative pathology Peritoneal Diseases pathology 1988 6 1 1988 6 1 0 1 1988 6 1 0 0 ppublish 3176478 PMC1026221 Ann Surg. 1965 Jun;161:864-75

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1988 Western Journal of Medicine

712. Case number 31: Nodular panniculitis as expression of Munchausen's syndrome (panniculitis artefacta) (PubMed)

Case number 31: Nodular panniculitis as expression of Munchausen's syndrome (panniculitis artefacta) 15361370 2004 10 25 2008 11 20 0003-4967 63 10 2004 Oct Annals of the rheumatic diseases Ann. Rheum. Dis. Case number 31: Nodular panniculitis as expression of Munchausen's syndrome (panniculitis artefacta). 1195-6 Tausche A-K AK Department of Rheumatology, University Clinic Carl Gustav Carus, Dresden Univarsity of Technology, Dresden, Germany. anne-kathrin.tausche@mailbox.tu-dresden.de Hänsel S (...) S Tausche K K Unger S S Schröder H E HE Pietsch J J eng Case Reports Journal Article England Ann Rheum Dis 0372355 0003-4967 IM Female Humans Middle Aged Munchausen Syndrome diagnosis Panniculitis, Nodular Nonsuppurative etiology pathology psychology 2004 9 14 5 0 2004 10 27 9 0 2004 9 14 5 0 ppublish 15361370 10.1136/ard.2004.024539 63/10/1195 PMC1754771

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2004 Annals of the Rheumatic Diseases

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