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Panniculitis

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701. Hepatosplenic and Subcutaneous Panniculitis-Like γ/δ T Cell Lymphomas Are Derived from Different Vδ Subsets of γ/δ T Lymphocytes Full Text available with Trip Pro

Hepatosplenic and Subcutaneous Panniculitis-Like γ/δ T Cell Lymphomas Are Derived from Different Vδ Subsets of γ/δ T Lymphocytes Gamma/delta T cell lymphomas (gamma/delta TCL) represent rare, often aggressive types of T cell malignancy that are clinically and pathologically diverse. Most gamma/delta TCL occur as a hepatosplenic or subcutaneous type. To date, analysis of the T cell receptor delta (TCRS) gene repertoire of hepatosplenic gamma/delta TCL (gamma/delta HSTCL) and subcutaneous (...) panniculitis-like gamma/delta TCL (gamma/delta SPTCL) has been reported only in a limited number of cases. In this study we analyzed 11 gamma/delta HSTCL and 4 gamma/delta SPTCL by polymerase chain reaction and immunostaining to determine their usage of the Vdelta subtypes (Vdelta1-6). It is noteworthy that 10 of 11 gamma/delta HSTCL expressed the Vdelta1 gene. The remaining case also expressed T cell receptor delta (TCRS) as determined by flow cytometry and TCRdelta rearrangement in Southern blot. However

2000 The Journal of molecular diagnostics : JMD

702. Recurrent panniculitis as the first clinical manifestation of recurrent acute pancreatitis secondary to cholelithiasis. Full Text available with Trip Pro

Recurrent panniculitis as the first clinical manifestation of recurrent acute pancreatitis secondary to cholelithiasis. A case of recurrent panniculitis in the legs as the first clinical manifestation of recurrent acute pancreatitis secondary to cholelithiasis is described in a 59-year-old Caucasian woman.

1996 Journal of the Royal Society of Medicine

703. Lupus panniculitis Full Text available with Trip Pro

Lupus panniculitis 9059148 1997 03 20 2008 11 20 0003-4967 56 1 1997 Jan Annals of the rheumatic diseases Ann. Rheum. Dis. Unusual but memorable. Systemic lupus erythematosus with panniculitis. 77 Wright G D GD City Hospital, Nottingham, UK. Powell R R Doherty M M eng Case Reports Journal Article England Ann Rheum Dis 0372355 0003-4967 IM Female Heel pathology Humans Lupus Erythematosus, Systemic complications pathology Middle Aged Panniculitis, Lupus Erythematosus complications pathology 1997

1997 Annals of the Rheumatic Diseases

704. Panniculitis: a report of four cases and literature review. Full Text available with Trip Pro

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.

1991 Archives of Disease in Childhood

705. Mesenteric panniculitis. Full Text available with Trip Pro

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

1988 Western Journal of Medicine

706. Weber-Christian panniculitis. Full Text available with Trip Pro

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.

1987 Annals of the Rheumatic Diseases

707. Nodular Panniculitis in a Female Toy Poodle Full Text available with Trip Pro

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.

1983 The Canadian Veterinary Journal

708. Treatment with cimetidine of atypical fasciitis panniculitis syndrome. Full Text available with Trip Pro

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.

1990 Annals of the Rheumatic Diseases

709. Lobular panniculitis associated with ciprofloxacin. Full Text available with Trip Pro

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

1990 BMJ : British Medical Journal

710. Granulomatous lipophagic panniculitis and temporal arteritis in a patient with cryptogenic chronic active hepatitis. Full Text available with Trip Pro

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.

1992 Annals of the Rheumatic Diseases

711. Pyogranulomatous panniculitis in a cat associated with infection by the Mycobacterium fortuitum/peregrinum group Full Text available with Trip Pro

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

2002 The Canadian Veterinary Journal

712. A pilot study of thalidomide for patients with symptomatic mesenteric panniculitis. (Abstract)

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

713. Nasal-type natural killer cell lymphoma preceded by benign panniculitis arising in an asymptomatic HTLV-1 carrier. (Abstract)

Nasal-type natural killer cell lymphoma preceded by benign panniculitis arising in an asymptomatic HTLV-1 carrier. We report a case of an Epstein-Barr virus (EBV)-associated nasal-type natural killer cell lymphoma (NKCL) preceded by benign panniculitis, which arose in a 48-year-old woman with an asymptomatic human T-cell leukemia/lymphoma virus type-1 (HTLV-1) infection. A biopsy of the initial panniculitis lesion demonstrated lobular panniculitis with a germinal center composed of benign (...) mononuclear cells with a phenotype of CD4+CD45RO+CD5sCD3+ cCD3 epsilon + T-cell intracellular antigen-1 (TIA-1)- and granzyme B-. One year after oral prednisolone therapy, the patient developed subcutaneous nodules composed of atypical lymphoid cells with a phenotype of CD4-CD45RO+CD56+sCD3-cCD3 epsilon + (TIA-1)+ and granzyme B+. In the initial panniculitis lesion, neither EBV-encoded RNA (EBER-1) nor clonal proliferation of EBV-infected cells was identified. In later lesions, however, a large number

2003 International Journal of Dermatology

714. Panniculitis secondary to extravasation of clarithromycin in a patient with alpha 1-antitrypsin deficiency (phenotype PiZ). (Abstract)

Panniculitis secondary to extravasation of clarithromycin in a patient with alpha 1-antitrypsin deficiency (phenotype PiZ). alpha 1-Antitrypsin deficiency (AATD) is known to be associated with panniculitis. Although reports of this association are rare, the true incidence may be unappreciated because of underdiagnosis of AATD. We report a case of panniculitis occurring in a 34-year-old woman with severe AATD following the extravasation of clarithromycin infused intravenously for treatment

2003 British Journal of Dermatology

715. Effective treatment of relapsing idiopathic nodular panniculitis (Pfeifer-Weber-Christian disease) with mycophenolate mofetil. (Abstract)

Effective treatment of relapsing idiopathic nodular panniculitis (Pfeifer-Weber-Christian disease) with mycophenolate mofetil. Relapsing idiopathic nodular panniculitis is the term used to describe a group of diseases that presents as subcutaneous inflammatory nodules, fever and systemic symptoms and histopathologically displays inflammation within the fat lobules. There is no specific test for diagnosis and extensive investigations are required to exclude systemic causes of panniculitis (...) . No uniform effective therapy is available and various drugs used include mainly corticosteroids alone or in combination with other immunosuppressive agents. Presented in this paper is an intractable case of idiopathic nodular panniculitis whose corticotherapy failed and could not be continued because of serious adverse effects. The rapid and good therapeutic response of the patient to mycophenolate mofetil monotherapy is discussed.

2003 Journal of Dermatological Treatment

716. Panniculitis-like T-cell lymphoma clinically manifested as alopecia. (Abstract)

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

717. Subcutaneous panniculitis-like T-cell lymphoma: a clinicopathological, immunophenotypic and molecular analysis of six patients. (Abstract)

Subcutaneous panniculitis-like T-cell lymphoma: a clinicopathological, immunophenotypic and molecular analysis of six patients. Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare cytotoxic T-cell lymphoma of the skin. In the World Health Organization classification of T-cell and natural killer cell lymphoma it is listed as an example of extranodal lymphoma. In practice, however, it is most likely to present to a dermatologist.To describe the clinicopathological, immunophenotypic

2003 British Journal of Dermatology

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

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

719. Panniculitis and lipodystrophy. (Abstract)

Panniculitis and lipodystrophy. Panniculitis and lipodystrophy are rare disorders of subcutaneous tissue. Recently the incidence of lipodystrophy has been increasing secondary to its appearance in patients with HIV. In this population, the lipodystrophy appears to be a direct consequence of drug therapy. A review of the available literature regarding pathogenesis and treatment options is discussed. The diagnosis of panniculitis has been hampered by problems. The recent literature has

2002 Current Opinion in Rheumatology

720. Case number 31: Nodular panniculitis as expression of Munchausen's syndrome (panniculitis artefacta) Full Text available with Trip Pro

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

2004 Annals of the Rheumatic Diseases

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