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21. Chronic pancreatitis with multiple pseudocysts and pancreatic panniculitis: A case report. Full Text available with Trip Pro

Chronic pancreatitis with multiple pseudocysts and pancreatic panniculitis: A case report. Pancreatic pseudocyst can present single or multiple, inside or outside the pancreas. Pancreatic panniculitis is a rare skin lesion in pancreatic disease patients. The purpose of this study is to report a case of chronic pancreatitis coexisting with multiple pseudocysts and pancreatic panniculitis.A 46-year-old man with chronic pancreatitis presented multiple small cystic lesions inside the head (...) of the pancreas and two large cystic lesions adjacent to the tail of the pancreas. The patient also developed subcutaneous nodules involving upper and lower limbs, hands, and lower abdomen bilaterally.The patient was diagnosed with pancreatic pseudocyst and pancreatic panniculitis resulted from chronic pancreatitis.Bile duct stent and pancreatic duct stent placement was performed endoscopicly.Panniculitis faded three weeks later and the pancreatic pseudocysts disappeared six weeks later.Clinicians should

2018 Medicine

22. Distinctive lupus panniculitis of scalp with linear alopecia along Blaschko's lines: a review of the literature. (Abstract)

Distinctive lupus panniculitis of scalp with linear alopecia along Blaschko's lines: a review of the literature. Lupus panniculitis of the scalp (LPS) is a rare and distinctive clinical feature of lupus erythematosus panniculitis (LEP) with linear alopecia along Blaschko's lines. In this study, we investigated clinical features and treatments of LPS by literature review of articles in the English language from PubMed and SCOPUS databases up to April 2018. The following key words, "lupus (...) panniculitis, "lupus erythematosus panniculitis", "lupus profundus", "head", and "scalp", were used. Twenty cases of LPS were identified (mean age = 26.4 [10-53] years, female: male ratio = 1:1, mean disease duration = 86.89 [8-336] weeks). The most commonly affected areas of scalp included parietal (70%), frontal (45%), temporal (40%), occipital (30%), and vertex (10%), along 70% of Blaschko's lines with morphologic lesions linear, annular, arch-shaped, and ulcer. Besides, ANA (60%) was in particular

2018 International Journal of Dermatology

23. Pancreatic panniculitis: A case series from a tertiary university hospital in Spain. (Abstract)

Pancreatic panniculitis: A case series from a tertiary university hospital in Spain. Pancreatic panniculitis is a rare type that only occurs in 2-3% of all patients with pancreatic diseases. It is usually described in association with benign pancreatic disease and less commonly in association with pancreatic carcinoma. We describe a case of pancreatic panniculitis as the first manifestation of underlying ampullary adenocarcinoma and a new case of pancreatitis, panniculitis and polyarthritis (...) (PPP-Syndrome). Pancreatic panniculitis may be the cutaneous manifestation of pancreatic allograft rejection after simultaneous pancreas-kidney transplantation.© 2018 The Australasian College of Dermatologists.

2018 Australasian Journal of Dermatology

24. Alpha-1 antitrypsin deficiency panniculitis: clinical and pathologic characteristics of 10 cases. (Abstract)

Alpha-1 antitrypsin deficiency panniculitis: clinical and pathologic characteristics of 10 cases. Alpha-1 antitrypsin deficiency (AATD) may be associated with liver and lung disease and rarely causes panniculitis.We evaluated the clinicopathologic and laboratory findings of AATD panniculitis in 10 patients.We conducted a retrospective review of all cases of AATD panniculitis at Mayo Clinic, Rochester, MN, from 1989 to 2016.Ten patients with AATD panniculitis were included. Seven of ten were (...) women. Clinical lesions were most commonly nodular (100%), erythematous (90%), ulcerated (90%), and painful (90%) subcutaneous nodules and plaques. Extracutaneous associations were rare. PiZZ phenotype was most commonly identified (50%). Histopathologically, lobular panniculitis (80%) with associated septal involvement (60%) and a predominant neutrophilic infiltrate (100%) were most common. Treatments varied; dapsone and alpha-1 proteinase inhibitor infusions were each used in five (50%) patients

2018 International Journal of Dermatology

25. Cold Panniculitis After Ice Therapy for Supraventricular Tachycardia. (Abstract)

Cold Panniculitis After Ice Therapy for Supraventricular Tachycardia. A late preterm infant presenting with supraventricular tachycardia (SVT) was admitted to the pediatric intensive care unit because of poor systolic function seen on echocardiogram. The hospitalization was complicated by multiple breakthrough episodes of SVT requiring ice placed on the face during each repeat episode. The infant was later diagnosed as having cold panniculitis secondary to the application of ice to the face (...) on multiple occasions. In children who are hemodynamically stable during SVT episodes, ice is used as first-line treatment. It is important to be aware of how often ice is being applied to the face and the duration of time to limit complications such as cold panniculitis.

2018 Pediatric Emergency Care

26. Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome. Full Text available with Trip Pro

Author Correction: Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome. In the version of this article originally published, the main-text sentence "In three patients of European ancestry, we identified the germline variant encoding p.Ile97Met in TIM-3, which was homozygous in two (P12 and P13) and heterozygous in one (P15) in the germline but with no TIM-3 plasma membrane expression in the tumor

2018 Nature Genetics

27. Relapsed subcutaneous panniculitis-like T cell lymphoma evaluated by FDG PET/CT: A clinical case report. Full Text available with Trip Pro

Relapsed subcutaneous panniculitis-like T cell lymphoma evaluated by FDG PET/CT: A clinical case report. Subcutaneous panniculitis-like T cell lymphoma (SPTCL) is a rare primary cutaneous T cell lymphomas expressing α/β T cell receptors that preferentially involves subcutis, and few reports have investigated the diagnosis of suspicious relapsed SPTCL using F-fluoro-2-deoxy-D-glucose (F-FDG) positron emission tomography/computed tomography (PET/CT).A 15-year-old woman complaining of a growing

2018 Medicine

28. Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome. (Abstract)

Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome. Subcutaneous panniculitis-like T cell lymphoma (SPTCL), a non-Hodgkin lymphoma, can be associated with hemophagocytic lymphohistiocytosis (HLH), a life-threatening immune activation that adversely affects survival1,2. T cell immunoglobulin mucin 3 (TIM-3) is a modulator of immune responses expressed on subgroups of T and innate immune cells. We

2018 Nature Genetics

29. Inherited Immunodeficiency: A New Association With Early-Onset Childhood Panniculitis. Full Text available with Trip Pro

Inherited Immunodeficiency: A New Association With Early-Onset Childhood Panniculitis. We report on 4 children who presented with aseptic panniculitis associated with inherited immunodeficiency. Three patients had a B-cell immunodeficiency resulting from mutations in the TRNT1 and NF-κb2 genes (no mutation was found in the third patient), and 1 had a T-cell deficiency (mutation in the LCK gene). Panniculitis occurred before the age of 2 years in the 4 patients and preceded the onset (...) of recurrent infections because of immunodeficiency in 2. It presented either as nodules, which resolved spontaneously within 1 to 2 weeks (3 patients), or chronic ulcerative lesions (1 patient) associated with unexplained fever and elevated acute phase reactants, without evidence of infection or high-titer autoantibodies. Febrile nodules relapsed in 2 patients, and recurrent attacks of unexplained fever (without relapse of panniculitis) occurred in the third. Skin biopsy revealed predominantly lympho

2018 Pediatrics

30. Dermatomyositis panniculitis: A clinico-pathologic and immunohistochemical study of 18 cases. (Abstract)

Dermatomyositis panniculitis: A clinico-pathologic and immunohistochemical study of 18 cases. Panniculitis occurring in dermatomyositis is uncommon, with only a few cases described in the literature, most of them as case reports.This report describes the clinicopathological and immunohistochemical findings in a series of 18 patients with panniculitis associated with dermatomyositis.In each patient, we collected the clinical data of the cutaneous lesions as well as the characteristic clinical (...) and laboratory findings. A series of histopathologic findings was recorded in the biopsy of each patient. A panel of antibodies was used in some cases to investigate the immunophenotype of the infiltrate. Data of treatment and follow-up were also collected.Of the 18 patients, 13 were female and 5 were male, ranging in age from 13 to 74 years (median, 46.4 years). In addition to panniculitis, all patients presented pathognomonic cutaneous findings of DM and reported proximal muscle weakness prior

2018 Journal of the European Academy of Dermatology and Venereology

31. Lupus erythematosus panniculitis in a 10-year-old female child with severe systemic lupus erythematosus: A case report. Full Text available with Trip Pro

Lupus erythematosus panniculitis in a 10-year-old female child with severe systemic lupus erythematosus: A case report. Lupus erythematosus panniculitis (LEP) is a rare subset of lupus erythematosus. The incidence of LEP in systemic lupus erythematosus (SLE) ranges from 2% to 5%. In the previous literature, most LEP patients were women aged from 20 to 60 years, while pediatric cases were rare, all of whom appeared on their own without SLE.A rare LEP in a 10-year-old female child with severe SLE

2018 Medicine

32. Mesenteric Panniculitis Presenting as Fever of Unknown Etiology in a Patient with History of Abdominal Surgery Full Text available with Trip Pro

Mesenteric Panniculitis Presenting as Fever of Unknown Etiology in a Patient with History of Abdominal Surgery Mesenteric panniculitis is characterized by nonspecific fibrous inflammation of the small bowel mesentery, appendix, and mesoappendix. Clinical course is usually benign and outcome is favorable. We report a case of mesenteric panniculitis presenting as fever of unknown etiology in a patient with history of abdominal surgery.

2018 Case reports in gastrointestinal medicine

33. Recurrent lupus profundus-like panniculitis associated with streptococcal throat infections in an immunocompetent child Full Text available with Trip Pro

Recurrent lupus profundus-like panniculitis associated with streptococcal throat infections in an immunocompetent child 29693070 2019 02 26 2352-5126 4 4 2018 May JAAD case reports JAAD Case Rep Recurrent lupus profundus-like panniculitis associated with streptococcal throat infections in an immunocompetent child. 359-361 10.1016/j.jdcr.2017.10.010 Min Michelle S MS Icahn School of Medicine at Mount Sinai, New York, New York. Boston University School of Medicine, Boston, Massachusetts. Phelps (...) Robert R Icahn School of Medicine at Mount Sinai, New York, New York. Levitt Jacob J Icahn School of Medicine at Mount Sinai, New York, New York. eng Case Reports 2018 04 04 United States JAAD Case Rep 101665210 2352-5126 EN, erythema nodosum LEP, lupus erythematosus profundus SLE, systemic lupus erythematosus Streptococcus infection lupus erythematosus profundus panniculitis 2018 4 26 6 0 2018 4 26 6 0 2018 4 26 6 1 epublish 29693070 10.1016/j.jdcr.2017.10.010 S2352-5126(17)30262-X PMC5911798

2018 JAAD Case Reports

34. Lobular panniculitis associated with chikungunya fever: A case report Full Text available with Trip Pro

Lobular panniculitis associated with chikungunya fever: A case report Chikungunya fever is a mosquito-borne viral disease classically characterized by an acute onset of fever, arthralgia, and skin rash. In this article, we report the acute febrile illness of an adult female with arthropathy and morbilliform eruptions. The patient developed panniculitis lesions on both shins. This report aims to describe an infrequent cutaneous presentation of chikungunya fever.

2018 IDCases

35. Useful Parameters for Distinguishing Subcutaneous Panniculitis-like T-Cell Lymphoma From Lupus Erythematosus Panniculitis. (Abstract)

Useful Parameters for Distinguishing Subcutaneous Panniculitis-like T-Cell Lymphoma From Lupus Erythematosus Panniculitis. Some cases of subcutaneous panniculitis-like T-cell lymphoma (SPTCL) and lupus erythematosus panniculitis (LEP) demonstrate clinical and histopathologic overlap, raising the possibility that they represent opposite ends of a disease spectrum. SPTCL, however, is typically associated with greater morbidity and risk for hemophagocytic lymphohistiocytosis (HLH); therefore

2016 American Journal of Surgical Pathology

36. Subcutaneous Panniculitis-Like T Cell Lymphoma Mimicking Early-Onset Nodular Panniculitis Full Text available with Trip Pro

Subcutaneous Panniculitis-Like T Cell Lymphoma Mimicking Early-Onset Nodular Panniculitis Subcutaneous panniculitis-like T cell lymphoma is a very uncommon subtype of cutaneous T cell lymphoma. The manifestations of this rare disease are atypical at onset, and may mimic some rheumatic or dermatologic diseases, which causes the delay of diagnosis and treatment.We report a 24-year-old man suffering from intermittent fever and skin nodules on the left anterior chest wall, who was initially (...) misdiagnosed with nodular panniculitis and finally diagnosed with subcutaneous panniculitis-like T cell lymphoma through repeat examination of biopsy of the skin nodule. Positron emission tomography revealed extracutaneous adipose tissue involvement. Subsequently, hemophagocytic syndrome occurred while under a conventional dose of glucocorticoid, but remission was induced by treatment with cyclosporine A and high doses of dexamethasone.In order to avoid the delay diagnosis and inappropriate treatment

2016 The American journal of case reports

37. Atypical lymphocytic lobular panniculitis: an overlap condition with features of subcutaneous panniculitis-like T-cell lymphoma and lupus profundus Full Text available with Trip Pro

Atypical lymphocytic lobular panniculitis: an overlap condition with features of subcutaneous panniculitis-like T-cell lymphoma and lupus profundus 27807018 2017 02 23 2018 11 13 1757-790X 2016 2016 Nov 02 BMJ case reports BMJ Case Rep Atypical lymphocytic lobular panniculitis: an overlap condition with features of subcutaneous panniculitis-like T-cell lymphoma and lupus profundus. bcr2016215335 10.1136/bcr-2016-215335 He Alice A http://orcid.org/0000-0002-1938-0619 Department of Dermatology (...) Antirheumatic Agents 4QWG6N8QKH Hydroxychloroquine Subcutaneous panniculitis-like T-cell lymphoma IM Antirheumatic Agents therapeutic use Biopsy Diagnosis, Differential Female Humans Hydroxychloroquine therapeutic use Lymphoma, T-Cell diagnosis drug therapy pathology Middle Aged Necrosis Panniculitis diagnosis drug therapy pathology Panniculitis, Lupus Erythematosus diagnosis drug therapy pathology Polymerase Chain Reaction Upper Extremity Conflicts of Interest: None declared. 2016 11 4 6 0 2017 2 24 6 0

2016 BMJ case reports

38. Mesenteric Panniculitis : Review of Consecutive Abdominal MDCT Examinations With a Matched-pair Analysis

Mesenteric Panniculitis : Review of Consecutive Abdominal MDCT Examinations With a Matched-pair Analysis Mesenteric Panniculitis : Review of Consecutive Abdominal MDCT Examinations With a Matched-pair Analysis - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100 (...) ). Please remove one or more studies before adding more. Mesenteric Panniculitis : Review of Consecutive Abdominal MDCT Examinations With a Matched-pair Analysis (MP - Cancer) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03316001 Recruitment Status : Completed First Posted : October 20, 2017 Last

2017 Clinical Trials

39. Diffuse granulomatous panniculitis associated with anti PD-1 antibody therapy Full Text available with Trip Pro

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

40. Increased levels of prostaglandin E-major urinary metabolite (PGE-MUM) in active mesenteric panniculitis patients: A case report. Full Text available with Trip Pro

Increased levels of prostaglandin E-major urinary metabolite (PGE-MUM) in active mesenteric panniculitis patients: A case report. Mesenteric panniculitis (MP) is a rare disease with abdominal and systemic symptoms and is characterized by nonspecific inflammation, fat necrosis, and fibrosis in mesenteric fat. Active inflammatory responses may increase levels of prostaglandin E-major urinary metabolite (PGE-MUM), which was reported to reflect the disease activity of ulcerative colitis and chronic (...) fibrosing interstitial pneumonia. We recently experienced a case with elevated PGE-MUM at the time of diagnosis of MP and we investigated the potential of PGE-MUM as a biomarker.In this report we described 2 active mesenteric panniculitis patients with high PGE-MUM levels.Mesenteric panniculitis INTERVENTIONS:: Both MP patients were measured the levels of PGE-MUM.Both MP patients exhibited high levels of PGE-MUM before treatment. In one, the levels were sensitively correlated with clinical symptoms

2017 Medicine

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