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Panniculitis

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61. Bilateral ptosis as first presentation of cytophagic histiocytic panniculitis: a case report. Full Text available with Trip Pro

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

62. An unusual location of gouty panniculitis: A case report. Full Text available with Trip Pro

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

63. Sclerosing mesenteritis and mesenteric panniculitis - clinical experience and radiological features. Full Text available with Trip Pro

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

64. Nilotinib-induced panniculitis in a patient with chronic myelogenous leukemia. (Abstract)

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

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

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

66. Panniculitis

Panniculitis Panniculitis Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Panniculitis Panniculitis Aka: Panniculitis II. Definition (...) Subcutaneous fat inflammation III. Causes: Mostly Septal ( of small veins) (thrombosis of large veins) Cutaneous (arteries and arterioles) No Necrobiotic xanthogranuloma Rheumatoid IV. Causes: Mostly Lobular Nodular Associated with Found on lower legs (Bazin disease) Panniculitis on the back of the calves Lucio's phenomenon ( ic lobular Panniculitis) No s Alpha-1 antitrypsin deficiency Pancreatic Panniculitis ( , ) Crystal deposition in fat Sclerema neonatorum of the newborn Post- Panniculitis Tissue

2018 FP Notebook

67. Purulent lupus panniculitis unmasked by FDG-PET/CT scan: A case report. Full Text available with Trip Pro

Purulent lupus panniculitis unmasked by FDG-PET/CT scan: A case report. Lupus panniculitis (LP) is a unique variant of cutaneous lupus erythematosus. Clinical manifestations are typically mild and include erythema, nodules, and small ulcers. In certain cases, diagnosing LP may be challenging. Skin overlying the typical subcutaneous inflammation may appear normal, and bacterial superinfections of the skin sometimes mask the underlying LP. It has been suggested that a computed tomography (CT

2016 Medicine

68. Crohn's disease mistaken for long-standing idiopathic mesenteric panniculitis: A case report and management algorithm. Full Text available with Trip Pro

Crohn's disease mistaken for long-standing idiopathic mesenteric panniculitis: A case report and management algorithm. Mesenteric panniculitis (MP) is mostly an associated sign of an intra-abdominal or systemic inflammatory primary disease. Nevertheless, etiological and differential diagnosis of idiopathic MP can be challenging when an associate primary cause is not in the foreground.We report here the case of an isolated small bowel Crohn's disease, long time considered as idiopathic MP.This

2016 Medicine

69. Neutrophilic panniculitis and autoinflammation: what's the link? (Abstract)

Neutrophilic panniculitis and autoinflammation: what's the link? 27035799 2017 10 10 2018 12 02 1365-2133 175 3 2016 09 The British journal of dermatology Br. J. Dermatol. Neutrophilic panniculitis and autoinflammation: what's the link? 646-7 10.1111/bjd.14606 Marzano A V AV 0000-0002-8160-4169 Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti, Università degli Studi di Milano, Unità Operativa di Dermatologia, IRCCS Fondazione Ca' Granda, Ospedale Maggiore Policlinico, Milan (...) Panniculitis 2016 4 2 6 0 2016 4 2 6 0 2017 10 11 6 0 ppublish 27035799 10.1111/bjd.14606

2016 British Journal of Dermatology

70. Case report of subcutaneous panniculitis-like T-cell lymphoma complicated by eyelid swelling. Full Text available with Trip Pro

Case report of subcutaneous panniculitis-like T-cell lymphoma complicated by eyelid swelling. Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare, highly malignant, extranodal lymphoma that preferentially infiltrates into subcutaneous adipose tissue. No case of SPTCL with the earliest symptoms occurring in the eye region has been reported. We report a case of SPTCL complicated by eyelid swelling.A 19-year-old Japanese man presented with worsening left eyelid swelling. The patient's (...) panniculitis, and inflammatory pseudotumor. Systemic antibiotics were initiated. The following day, he underwent a sub-Tenon's injection of triamcinolone. Left eyelid swelling gradually improved. He was discharged on the ninth day and followed up with oral prednisolone. Two months later, he visited our department because of a high fever and slight right eyelid swelling. Ocular hypertension was detected. A blood examination revealed pancytopenia. Computed tomography showed fluid retention, hydrothorax

2016 BMC Ophthalmology

71. Subcutaneous Panniculitis-like T cell Lymphoma: Immunosuppressive Drugs Induce Better Response than Polychemotherapy. Full Text available with Trip Pro

Subcutaneous Panniculitis-like T cell Lymphoma: Immunosuppressive Drugs Induce Better Response than Polychemotherapy. Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is a rare condition usually considered to have a favourable prognosis. However, it is not known whether polychemotherapy or immunosuppressive-based therapy is the best approach for treating SPTCL. Using data collected between 2000 and 2012 in France, we analysed clinical, biological and pathological data of 27 patients (...) with SPTCL. Medical history revealed that 40% of patients had been previously diagnosed with an autoimmune disorder and 22% with inflammatory panniculitis. Haemophagocytic syndrome was present in 37% of cases. Autoantibodies were positive in 65% of cases. Complete remission (CR) was reached in 74% of cases. Immunosuppressive drug treatment was given in 69.5% of patients (group 1) and polychemotherapy in 30.5% (group 2). CR was 81.2% and 28.5% (p?=?0.025), respectively. Progression rate was 6.2% and 42.8

2016 Acta Dermato-Venereologica

72. Lupus Panniculitis as an Initial Manifestation of Systemic Lupus Erythematosus: A Case Report. Full Text available with Trip Pro

Lupus Panniculitis as an Initial Manifestation of Systemic Lupus Erythematosus: A Case Report. Lupus erythematosus panniculitis (LEP) is a variant of chronic cutaneous lupus erythematosus (CCLE). Reported cases of LEP lesions before the diagnosis of systemic lupus erythematosus (SLE) were very rare; only 9 cases have been reported, to the best of our knowledge. We now describe the case of a 19-year-old male patient, with an overall review of the English literature. In the earliest stage

2016 Medicine

73. Pancreatic panniculitis in a patient with pancreatic-type acinar cell carcinoma of the liver - case report and review of literature. Full Text available with Trip Pro

Pancreatic panniculitis in a patient with pancreatic-type acinar cell carcinoma of the liver - case report and review of literature. Pancreatic panniculitis is a rare condition, which has only been described in relation with pancreatic diseases up to now. It is characterized by necrotizing subcutaneous inflammation and is thought to be triggered by adipocyte necrosis due to systemic release of pancreatic enzymes with consecutive infiltration of neutrophils. We present the first case (...) of a patient with pancreatic panniculitis caused by pancreatic-type primary acinar cell carcinoma (ACC) of the liver and without underlying pancreatic disease.A 73-year old Caucasian female patient was referred to our department with painful cutaneous nodules persisting for eight weeks and with marked lipasemia (~15000 U/l; normal range <60 U/l). Four weeks prior, several liver lesions had been detected. Empiric treatment with steroids did not show any effect. A biopsy of the skin nodules revealed

2016 BMC Cancer

74. Long-term remission of subcutaneous panniculitis-like T-cell lymphoma with central nervous system involvement: A case report Full Text available with Trip Pro

Long-term remission of subcutaneous panniculitis-like T-cell lymphoma with central nervous system involvement: A case report Subcutaneous panniculitis-like T-cell lymphoma (SPTCL) is an indolent cutaneous T-cell lymphoma with a favourable prognosis. The reported incidence of central nervous system (CNS) involvement in SPTCL is extremely low. SPTCL with CNS involvement is a fatal disease with no optimal treatment. The present study presents the case of a 27-year-old man who initially presented

2016 Oncology letters

75. Fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography evaluation of subcutaneous panniculitis-like T cell lymphoma and treatment response Full Text available with Trip Pro

Fluorine-18 fluorodeoxyglucose positron emission tomography/computed tomography evaluation of subcutaneous panniculitis-like T cell lymphoma and treatment response Subcutaneous panniculitis-like T cell lymphoma (SPTCL) is a very rare variant of non-Hodgkin's lymphoma. Currently, there is no standard imaging method for staging of SPTCL nor for assessment of treatment response. Here, we describe our use of fluorine-18 fluorodeoxyglucose (FDG) positron emission tomography/computed tomography (PET

2016 World journal of clinical cases

76. Pancreatic disease, panniculitis, polyarthrtitis syndrome successfully treated with total pancreatectomy: Case report and literature review Full Text available with Trip Pro

Pancreatic disease, panniculitis, polyarthrtitis syndrome successfully treated with total pancreatectomy: Case report and literature review Pancreatic disease can be complicated by extrabdominal manifestations such as panniculitis and polyarthritis. The symptomatic triad comprising pancreatic disease, panniculitis and polyarthritis is also known as PPP syndrome and is characterized by severe chronic sequels and high mortality rate. We describe a case of PPP syndrome successfully treated (...) with spleen preserving total pancreatectomy; in addition we performed a literature review.A 67 years old male presented panniculitis and polyarthritis without clinical abdominal symptoms. Clinical presentation, laboratory values and radiological findings demonstrated an acute pancreatitis and a pancreatic cancer was suspected; failure of conservatory treatments and high suspicious of malignancy led to perform a spleen preserving total pancreatectomy. Finally histological examination excluded a pancreatic

2016 International journal of surgery case reports

77. Mesenteric Panniculitis in a Thirteen-Year-Old Korean Boy Treated with Prednisolone: A Case Report Full Text available with Trip Pro

Mesenteric Panniculitis in a Thirteen-Year-Old Korean Boy Treated with Prednisolone: A Case Report Pediatric mesenteric panniculitis is an extremely rare disease of unknown etiology characterized by chronic inflammation, fat necrosis, and fibrosis in the mesenteric adipose tissue. A previously healthy 13-year-old boy was admitted because of right upper abdominal pain. An abdominal computed tomography scan revealed increased attenuation and enhancement in the left upper abdominal omental fat (...) and anterior peritoneal wall thickening. A laparoscopic biopsy showed mesenteric panniculitis with chronic inflammation, adiponecrosis, and septal fibrosis. Serological tests for autoimmune diseases, nested polymerase chain reaction for Mycobacterium tuberculosis, and special immunohistochemical stains for malignancy were all negative. Symptomatic improvement and improved abnormal findings were achieved after an 8-month treatment with prednisolone according to a follow-up abdominal computed tomography scan

2016 Pediatric gastroenterology, hepatology & nutrition

78. Pancreatic panniculitis preceding acute pancreatitis and subsequent detection of an intraductal papillary mucinous neoplasm: A case report Full Text available with Trip Pro

Pancreatic panniculitis preceding acute pancreatitis and subsequent detection of an intraductal papillary mucinous neoplasm: A case report 27408933 2016 07 13 2019 02 26 2352-5126 2 3 2016 May JAAD case reports JAAD Case Rep Pancreatic panniculitis preceding acute pancreatitis and subsequent detection of an intraductal papillary mucinous neoplasm: A case report. 244-6 10.1016/j.jdcr.2016.05.001 Menzies Stephanie S Department of Dermatology, St James's Hospital, Dublin, Ireland. McMenamin Mairin (...) pancreatitis intraductal papillary mucinous neoplasm pancreatic panniculitis 2016 7 14 6 0 2016 7 14 6 0 2016 7 14 6 1 epublish 27408933 10.1016/j.jdcr.2016.05.001 S2352-5126(16)30027-3 PMC4927540 Arch Dermatol. 1975 Apr;111(4):497-502 1122151 Arch Dermatol. 1976 Jul;112(7):993-4 132903 Dermatology. 2004;208(3):265-7 15118385 J Cutan Pathol. 2011 Jun;38(6):455-7 21521354 J Am Acad Dermatol. 1995 Sep;33(3):413-7 7657863 Am J Gastroenterol. 1990 Aug;85(8):1025-8 2375312 J Am Acad Dermatol. 1996 Aug;35(2 Pt 1

2016 JAAD Case Reports

79. Mycobacterial panniculitis caused by Mycobacterium thermoresistibile in a cat Full Text available with Trip Pro

Mycobacterial panniculitis caused by Mycobacterium thermoresistibile in a cat A domestic shorthair cat was evaluated for chronic, bilateral, ulcerative dermatitis affecting the inguinal region and lateral aspects of both pelvic limbs. Histopathologic examination of skin biopsies collected throughout the course of disease revealed chronic pyogranulomatous ulcerative dermatitis. Aerobic bacterial skin cultures yielded growth of a methicillin-resistant Staphylococcus aureus and Corynebacterium (...) panniculitis have been reported in cats. In the only detailed report of feline M thermoresistibile panniculitis, treatment was not attempted. The second case only reported detection of M thermoresistibile by PCR without a clinical description of the case. In our case report, severe chronic skin infection with M thermoresistibile was addressed using prolonged specific antibiotic therapy, surgical debridement and reconstructions, and treatment of secondary bacterial infections.

2016 JFMS Open Reports

80. Panniculitis caused by Mycobacterium monacense mimicking erythema induratum: a case in Ecuador Full Text available with Trip Pro

Panniculitis caused by Mycobacterium monacense mimicking erythema induratum: a case in Ecuador We report the first case of recently characterized species M. monacense associated with chronic nodular vasculitis, infecting a young woman. This case represents the first isolation of M. monacense from Ecuador. The isolate was identified by conventional and molecular techniques.

2016 New Microbes and New Infections

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