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41. Sclerosing mesenteritis and mesenteric panniculitis - clinical experience and radiological features. (Full text)

Sclerosing mesenteritis and mesenteric panniculitis - clinical experience and radiological features. Sclerosing mesenteritis (SM) is sometimes used as an umbrella-term for idiopathic inflammatory conditions in the mesentery. Mesenteric panniculitis (MP) is a radiological finding and its relation to clinical SM is not fully understood. The aims of this study were to determine whether any correlation could be found between the radiological findings and the clinical disease course.Patients

2017 BMC Gastroenterology PubMed

42. Bilateral ptosis as first presentation of cytophagic histiocytic panniculitis: a case report. (Full text)

Bilateral ptosis as first presentation of cytophagic histiocytic panniculitis: a case report. Cytophagic histiocytic panniculitis (CHP) is a rare form of nodular panniculitis that may progress to panniculitis-like T-cell lymphoma. We report a case of CHP that first manifested as bilateral ptosis, which is the first reported case of this presentation.A 25-year-old woman without medical history was referred to the neurology department of our hospital for evaluation of bilateral ptosis. Three (...) months previously, she suddenly complained of bilateral ptosis without apparent cause. Simultaneously, non-painful tender subcutaneous nodules and eschar-like skin lesions were observed on her extremities and trunk. A diagnosis of CHP was made based on skin biopsy from the left thigh showing lobular panniculitis, vasculitis, and adiponecrosis, with infiltration of inflammatory cells, including lymphocytes, histiocytes, and phagocytic histiocytes. Her condition continued to worsen with corticosteroid

2017 BMC Ophthalmology PubMed

43. Alpha-1-antitrypsin deficiency-related panniculitis: two cases with diverse clinical courses. (PubMed)

Alpha-1-antitrypsin deficiency-related panniculitis: two cases with diverse clinical courses. Alpha-1-antitrypsin deficiency (AATD)-related panniculitis is an extremely rare and underdiagnosed entity, and there is a paucity of data on its treatment. We report two cases of AATD-related panniculitis. The first was a 24-year-old woman with known AATD who presented with painful leg ulcers refractory to treatment with corticosteroids and colchicine. She had a good response to α1-antitrypsin (...) infusions but required dose adjustment due to flares in disease activity. The second case was a 38-year-old woman who presented with painful nodules on the legs refractory to corticosteroid therapy. Laboratory investigations revealed severe AATD. She had an excellent response to colchicine therapy. In both these cases of AATD, panniculitis was the first clinical manifestation of the disease. AATD-related panniculitis may have none of the typical clinical clues for AATD, such as a family history

2017 Clinical & Experimental Dermatology

44. An unusual location of gouty panniculitis: A case report. (Full text)

An unusual location of gouty panniculitis: A case report. Gouty panniculitis, characterised by the deposition of monosodium urate crystals in subcutaneous tissue, is a rare clinical manifestation of gout.The case of a 67-year-old man is reported, who presented an erythematous nodule on the upper part of the right buttock suspicious for an abscess. This was in the context of chemotherapy for non-Hodgkin's lymphoma.Histopathologic examination demonstrated gouty panniculitis.Because infection (...) intention. The patient was instructed to continue anti-hyperuricaemic treatment.In patients known to have long-standing hyperuricaemia and gout with nonspecific subcutaneous erythematous nodules, gouty panniculitis should be considered.

2017 Medicine PubMed

45. Nilotinib-induced panniculitis in a patient with chronic myelogenous leukemia. (PubMed)

Nilotinib-induced panniculitis in a patient with chronic myelogenous leukemia. 28319280 2017 09 14 1468-3083 31 9 2017 Sep Journal of the European Academy of Dermatology and Venereology : JEADV J Eur Acad Dermatol Venereol Nilotinib-induced panniculitis in a patient with chronic myelogenous leukaemia. e418-e419 10.1111/jdv.14232 Kitayama N N Department of Dermatology, Japanese Red Cross Wakayama Medical Center, Wakayama, 640-8558, Japan. Department of Dermatology, Kyoto University Graduate

2017 Journal of the European Academy of Dermatology and Venereology

46. Cutaneous Gamma-delta T-cell Lymphoma with an Initially Indolent Course Mimicking Lupus Panniculitis. (Full text)

Cutaneous Gamma-delta T-cell Lymphoma with an Initially Indolent Course Mimicking Lupus Panniculitis. 28175923 2018 04 17 2018 04 17 1651-2057 97 5 2017 05 08 Acta dermato-venereologica Acta Derm. Venereol. Cutaneous Gamma-delta T-cell Lymphoma with an Initially Indolent Course Mimicking Lupus Panniculitis. 665-666 10.2340/00015555-2630 Benecke Johannes J Department of Dermatology, Venereology and Allergy, University Medical Center Mannheim, Ruprecht-Karls-University of Heidelberg, Mannheim (...) , Germany. Géraud Cyrill C Nicolay Jan P JP eng Case Reports Journal Article Sweden Acta Derm Venereol 0370310 0001-5555 0 Receptors, Antigen, T-Cell, gamma-delta IM Aged Diagnosis, Differential Fatal Outcome Female Humans Lymphoma, T-Cell, Cutaneous diagnosis pathology Panniculitis, Lupus Erythematosus diagnosis Receptors, Antigen, T-Cell, gamma-delta metabolism Skin Neoplasms diagnosis pathology T-Lymphocytes metabolism 2017 2 9 6 0 2018 4 18 6 0 2017 2 9 6 0 ppublish 28175923 10.2340/00015555-2630

2017 Acta Dermato-Venereologica PubMed

47. Subcutaneous Panniculitis-Like T-Cell Lymphoma Presenting as a Local Inflammation of a Thigh in an 8-Month-Old Child (Full text)

Subcutaneous Panniculitis-Like T-Cell Lymphoma Presenting as a Local Inflammation of a Thigh in an 8-Month-Old Child During infancy, skin inflammation is usually treated in basic pediatric care. In this study, we present a case of an 8-month-old girl with a 2-month history of an inflammation of the thigh treated locally by ointments and oral antibiotics in basic and dermatological care. The patient had a history of fever, sweating, and failure to thrive. The lactate dehydrogenase was elevated (...) up to 869 U/L with low C-reactive protein (1.04 mg/L). Magnetic resonance imaging of the thigh reassured the diagnosis of local inflammation. Intravenous antibiotic caused mild local improvement, but the episodes of high fever sustained. The patient was transferred to our pediatric surgery department for treatment and surgical biopsy of the lesion. Histopathological examination confirmed a subcutaneous panniculitis-like T-cell lymphoma, which is a rare cytotoxic T-cell lymphoma representing less

2017 European Journal of Pediatric Surgery Reports PubMed

48. An Overlooked Potentially Treatable Disorder: Idiopathic Mesenteric Panniculitis (Full text)

An Overlooked Potentially Treatable Disorder: Idiopathic Mesenteric Panniculitis The aim of this study was to determine the prevalence of mesenteric panniculitis (MP) and to describe its clinical characteristics, therapy, and outcome.This retrospective study was carried out among patients with MP based on computed tomography (CT) scans from January 2012 to December 2015. The CT images were reanalyzed by study radiologists to confirm the previous MP diagnosis. Patients were divided into 2 groups

2017 Medical Principles and Practice PubMed

49. Intravascular large B-cell lymphoma presenting as panniculitis (Full text)

Intravascular large B-cell lymphoma presenting as panniculitis 29296641 2019 02 26 2352-5126 3 6 2017 Nov JAAD case reports JAAD Case Rep Intravascular large B-cell lymphoma presenting as panniculitis. 536-538 10.1016/j.jdcr.2017.06.032 Maiolo Corinne C Department of Dermatology, Royal Adelaide Hospital, Adelaide, Australia. Ibbetson S Jan SJ Department of Anatomical Pathology, SA Pathology, Adelaide, Australia. Sidhu Shireen K SK Department of Dermatology, Royal Adelaide Hospital, Adelaide (...) , Australia. Kearney Daniel D Department of Anatomical Pathology, SA Pathology, Adelaide, Australia. eng Case Reports 2017 11 06 United States JAAD Case Rep 101665210 2352-5126 B-cell lymphoma IVLBCL, Intravascular large B-cell lymphoma cutaneous lymphoma fat necrosis intravascular lymphoma panniculitis retiform purpura 2018 1 4 6 0 2018 1 4 6 0 2018 1 4 6 1 epublish 29296641 10.1016/j.jdcr.2017.06.032 S2352-5126(17)30144-3 PMC5728488 Int J Dermatol. 2009 Dec;48(12 ):1349-52 20415677 J Clin Oncol. 2007

2017 JAAD Case Reports PubMed

50. Diffuse granulomatous panniculitis associated with anti PD-1 antibody therapy (Full text)

Diffuse granulomatous panniculitis associated with anti PD-1 antibody therapy 29296642 2019 02 26 2352-5126 4 1 2018 Jan JAAD case reports JAAD Case Rep Diffuse granulomatous panniculitis associated with anti PD-1 antibody therapy. 13-16 10.1016/j.jdcr.2017.06.014 Jiang Baijia B California Pacific Medical Center, San Francisco, California. Patino Maria M MM California Pacific Medical Center, San Francisco, California. Gross Andrew J AJ University of California San Francisco, San Francisco (...) immune-related melanoma nivolumab panniculitis 2018 1 4 6 0 2018 1 4 6 0 2018 1 4 6 1 epublish 29296642 10.1016/j.jdcr.2017.06.014 S2352-5126(17)30126-1 PMC5739149 Cutis. 1978 Jun;21(6):806-10 657838 JAAD Case Rep. 2016 Jul 14;2(3):264-8 27486590 J Dermatol. 2014 Sep;41(9):817-20 24617955 Eur J Dermatol. 2015 Apr;25(2):177-80 25788221 Ann Dermatol Venereol. 2011 Feb;138(2):135-9 21333826 N Engl J Med. 2015 Jan 22;372(4):320-30 25399552 JAAD Case Rep. 2017 Apr 14;3(3):208-211 28443311 Lancet Oncol

2017 JAAD Case Reports PubMed

51. Remission of subcutaneous panniculitis-like T-cell lymphoma in a pregnant woman after treatment with oral corticosteroids as monotherapy (Full text)

Remission of subcutaneous panniculitis-like T-cell lymphoma in a pregnant woman after treatment with oral corticosteroids as monotherapy Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare form of cutaneous T-cell lymphoma characterized by neoplastic α/β T cells infiltrating subcutaneous tissues in a lobular pattern. Few data support the optimal treatment regimen for patients, given the rarity of this condition, and even fewer data describe treatment when diagnosed during pregnancy

2017 JAAD Case Reports PubMed

52. Panniculitis Associated with MEK Inhibitor Therapy: An Uncommon Adverse Effect (Full text)

Panniculitis Associated with MEK Inhibitor Therapy: An Uncommon Adverse Effect The combination of MEK inhibitor (cobimetinib, trametinib) and BRAF inhibitor (vemurafenib, dabrafenib) is now the first-line treatment in patients with BRAF V600-mutated metastatic melanoma. This association reduces cutaneous adverse events induced by BRAF inhibitors alone, including photosensitivity, hand-foot syndrome, hyperkeratosis, alopecia, skin papillomas, keratoacanthomas, and squamous-cell carcinomas. While (...) panniculitis has exceptionally been reported with BRAF inhibitors, this rare side effect has never been described with the use of MEK inhibitors. We present here the first observation of panniculitis strictly induced by MEK inhibitors. Indeed, 10 days after the initiation of combined treatment with cobimetinib and vemurafenib for metastatic melanoma, our patient developed panniculitis predominantly on the upper and lower extremities. These cutaneous nodules disappeared during cobimetinib intermissions

2017 Case reports in dermatology PubMed

53. Lysinibacillus massiliensis Panniculitis Masquerading as Erythema Nodosum: A Case Report (Full text)

Lysinibacillus massiliensis Panniculitis Masquerading as Erythema Nodosum: A Case Report Lysinibacillus massiliensis, formerly Bacillus massiliensis, is an environmental Gram-positive bacillus that is generally non-pathogenic. Rare case reports in immunosuppressed patients have described sepsis with this organism. In this study, we report a case of L massiliensis as a cause of infectious panniculitis mimicking erythema nodosum after infusion of autologous adipose-derived stem cells

2017 Open forum infectious diseases PubMed

54. Pancreatic acinar cell carcinoma presenting with panniculitis, successfully treated with FOLFIRINOX: A case report (Full text)

Pancreatic acinar cell carcinoma presenting with panniculitis, successfully treated with FOLFIRINOX: A case report Pancreatic acinar cell carcinoma (PACC) is a rare tumor of the exocrine pancreas, representing only 1% of all pancreatic malignancies. A 50-year-old man presented with edema of the thumb joints bilaterally, followed by an appearance of masses in the bilateral lower extremities and fever (38°C). The masses were diagnosed as panniculitis by skin biopsy, and multiple intraperitoneal (...) of the TNM Classification of Malignant Tumors). Combined chemotherapy with oxaliplatin, irinotecan and fluorouracil (FOLFIRINOX) was administered and fever was soon alleviated. The serum levels of lipase also declined and panniculitis completely resolved. As of the start of the 8th course of chemotherapy, the levels of the pancreatic exocrine enzymes were within normal ranges and CT revealed partial response. Therefore, the severe lipase hypersecretion syndrome was well controlled by the FOLFIRINOX

2017 Molecular and clinical oncology PubMed

55. Lupus erythematosus panniculitis resistant to standard treatment, complicated with macrophage activation syndrome (Full text)

Lupus erythematosus panniculitis resistant to standard treatment, complicated with macrophage activation syndrome 28670262 2018 11 13 1642-395X 34 3 2017 Jun Postepy dermatologii i alergologii Postepy Dermatol Alergol Lupus erythematosus panniculitis resistant to standard treatment, complicated with macrophage activation syndrome. 281-283 10.5114/ada.2017.67852 Juczynska Katarzyna K Department of Dermatology and Venereology, Medical University of Lodz, Lodz, Poland. Wozniacka Anna A Department

2017 Advances in Dermatology and Allergology/Postȩpy Dermatologii i Alergologii PubMed

56. Pancreatitis, panniculitis and polyarthritis (PPP-) syndrome caused by post-pancreatitis pseudocyst with mesenteric fistula. Diagnosis and successful surgical treatment. Case report and review of literature (Full text)

Pancreatitis, panniculitis and polyarthritis (PPP-) syndrome caused by post-pancreatitis pseudocyst with mesenteric fistula. Diagnosis and successful surgical treatment. Case report and review of literature Pancreatitis, panniculitis and polyarthritis syndrome is a very rare extra-pancreatic complication of pancreatic diseases.While in most cases this syndrome is caused by acute or chronic pancreatitis, we report a case of a 62-year-old man presenting with extensive intraosseous fat necrosis (...) , polyarthritis and panniculitis caused by a post-pancreatitis pseudocyst with a fistula to the superior mesenteric vein and extremely high blood levels of lipase. This became symptomatic 2.5 years after an episode of acute pancreatitis and as in most cases abdominal symptoms were absent. Treatment by surgical resection of the pancreatic head with the pseudocyst and mesenteric fistula led to complete remission of all symptoms.A review of the literature revealed that all publications are limited to case

2017 International journal of surgery case reports PubMed

57. Subcutaneous panniculitis-like T-cell lymphoma (Full text)

Subcutaneous panniculitis-like T-cell lymphoma Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare form of skin lymphoma that is localized primarily to the subcutaneous adipose tissue without involvement of the lymph nodes. Clinically, the skin lesions mimic lipomas, while histologically they resemble panniculitis. We report a case of a young woman with SPTCL. She achieved complete remission after combination chemotherapy.

2017 Proceedings (Baylor University. Medical Center) PubMed

58. An Unexpected Etiology of Pancreatic Panniculitis: A Case Report (Full text)

An Unexpected Etiology of Pancreatic Panniculitis: A Case Report Pancreatic panniculitis is a rare cause of subcutaneous fat necrosis secondary to elevated serum levels of pancreatic enzymes. It is most often associated with pancreatic acinar cell carcinoma, but has also been seen in patients with pancreatitis.We present a case of a 64 year old Caucasian man without symptoms of pancreatitis who presents with pancreatic panniculitis manifesting in multiple subcutaneous ulcerating nodules (...) of the bilateral lower extremities, discovered to have a previously unreported etiology for this condition. He had no evidence of pancreatitis or malignancy, but instead a pancreatic-portal fistula resulting in panniculitis.Peripancreatic vascular lesions must also be considered in the differential diagnosis of pancreatic panniculitis. The diagnosis, pathology, and treatment of pancreatic panniculitis are reviewed herein.

2017 Journal of Pancreatic Cancer PubMed

59. Mesenteric panniculitis (Full text)

Mesenteric panniculitis A 53-year-old black woman presented with a 3-day history of abdominal pain. Ultrasound of the abdomen showed a gall bladder packed with small stones. She gave a history of abdominal surgery for a gynaecological condition. She had a cholecystectomy done, but her symptoms continued after cholecystectomy. She then had anendoscopic retrograde cholangiopancreatogram (ERCP) and sphincterotomy done, again her symptoms remained the same. A CT scan of the abdomen was done (...) , and mesenteric panniculitis was suspected. A laparoscopic biopsy of the mesentery was performed, and it confirmed mesenteric panniculitis. She was started on a 2-week course of steroids to which she responded very well. Three months after the initial presentation, she was still asymptomatic.© BMJ Publishing Group Ltd (unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

2017 BMJ case reports PubMed

60. Successful treatment of hydroxyurea-associated panniculitis and vasculitis with low-dose methotrexate (Full text)

Successful treatment of hydroxyurea-associated panniculitis and vasculitis with low-dose methotrexate 28932785 2019 02 26 2352-5126 3 5 2017 Sep JAAD case reports JAAD Case Rep Successful treatment of hydroxyurea-associated panniculitis and vasculitis with low-dose methotrexate. 422-424 10.1016/j.jdcr.2017.06.009 Mattessich Sarah S University of Connecticut School of Medicine, Farmington, Connecticut. Ferenczi Katalin K Department of Dermatology, University of Connecticut, Farmington (...) , Connecticut. Lu Jun J Department of Dermatology, University of Connecticut, Farmington, Connecticut. eng Case Reports 2017 09 08 United States JAAD Case Rep 101665210 2352-5126 hydroxyurea methotrexate panniculitis vasculitis 2017 9 22 6 0 2017 9 22 6 0 2017 9 22 6 1 epublish 28932785 10.1016/j.jdcr.2017.06.009 S2352-5126(17)30121-2 PMC5594232 Curr Opin Rheumatol. 1999 May;11(3):226-32 10328583 Curr Hematol Malig Rep. 2006 Jun;1(2):69-74 20425334 Ann Hematol. 2015 Jun;94(6):901-10 25832853 Clin Exp

2017 JAAD Case Reports PubMed

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