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https://www.readbyqxmd.com/read/29744123/erythema-nodosum-as-sign-of-primary-tuberculosis
#1
Eleftherios Kritsotakis
Erythema nodosum is a panniculitis associated with numerous diseases such as infections, inflammatory diseases, tuberculosis or can be idiopathic. We here report a case of a woman with erythema nodosum and reactive arthritis who was subsequently diagnosed with tuberculosis. A high level of suspicion and a thorough clinical and laboratory investigation of the patient presenting with erythema nodosum is required, in order to detect a possible systemic underlying condition.
August 2017: Oxford Medical Case Reports
https://www.readbyqxmd.com/read/29742552/subcutaneous-panniculitis-like-t-cell-lymphoma-versus-lupus-erythematosus-panniculitis-distinction-by-means-of-the-periadipocytic-cell-proliferation-index
#2
Panitta Sitthinamsuwan, Penvadee Pattanaprichakul, Jitsupa Treetipsatit, Tawatchai Pongpruttipan, Sanya Sukpanichnant, Laura B Pincus, Timothy H McCalmont
The distinction between subcutaneous panniculitis-like T-cell lymphoma (SPTCL) and lupus erythematosus (LE) panniculitis is remarkably challenging. Rimming by lymphocytes with an elevated Ki-67 cell proliferation index has been forwarded as a potential diagnostic finding in biopsies of SPTCL but has not been rigorously compared with biopsies from patients with LE panniculitis. Nineteen and 17 examples of SPTCL and LE panniculitis, respectively, were evaluated for periadipocytic rimming by lymphocytes expressing Ki-67, CD8, and βF1 and for attributes associated with LE, including clusters of CD123-positive cells...
May 2, 2018: American Journal of Dermatopathology
https://www.readbyqxmd.com/read/29741276/pancreatic-panniculitis-a-case-series-from-a-tertiary-university-hospital-in-spain
#3
Clara Fernández-Sartorio, Andrea Combalia, Joan Ferrando, Mercè Alsina, Pilar Iranzo, Teresa Estrach, Eugenia Hernández-Ruiz, José M Mascaró
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...
May 9, 2018: Australasian Journal of Dermatology
https://www.readbyqxmd.com/read/29720803/unilateral-limb-thinning-thinking-out-of-the-box
#4
Chandramouleeswaran Venkatraman, Shubha Subramanian, Daniel Sweetson Abraham, Kannan Vellaichamy
We report an unusual presentation in a 9-year-old girl with unilateral circumferential thinning of the entire right upper limb without any other neurological deficit, with normal nerve conduction and electromyography initially thought of as a neurodegenerative disorder based on clinical presentation. Magnetic resonance imaging of the upper limb showed partial lipoatrophy with normal glucose metabolism and lipid profile and negativity for HIV and autoimmune disease (panniculitis) with no family history of similar disorder...
January 2018: Annals of Indian Academy of Neurology
https://www.readbyqxmd.com/read/29707779/alpha-1-antitrypsin-deficiency-panniculitis-clinical-and-pathologic-characteristics-of-10-cases
#5
Emma F Johnson, Stanislav N Tolkachjov, Lawrence E Gibson
BACKGROUND: Alpha-1 antitrypsin deficiency (AATD) may be associated with liver and lung disease and rarely causes panniculitis. OBJECTIVE: We evaluated the clinicopathologic and laboratory findings of AATD panniculitis in 10 patients. METHODS: We conducted a retrospective review of all cases of AATD panniculitis at Mayo Clinic, Rochester, MN, from 1989 to 2016. RESULTS: Ten patients with AATD panniculitis were included...
April 29, 2018: International Journal of Dermatology
https://www.readbyqxmd.com/read/29698337/cold-panniculitis-after-ice-therapy-for-supraventricular-tachycardia
#6
Laurie Malia, Alicia Wang, Laurie Scheiner, V Matt Laurich
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...
April 25, 2018: Pediatric Emergency Care
https://www.readbyqxmd.com/read/29693070/recurrent-lupus-profundus-like-panniculitis-associated-with-streptococcal-throat-infections-in-an-immunocompetent-child
#7
Michelle S Min, Robert Phelps, Jacob Levitt
No abstract text is available yet for this article.
May 2018: JAAD Case Reports
https://www.readbyqxmd.com/read/29693065/cold-panniculitis-adverse-cutaneous-effect-of-whole-body-cryotherapy
#8
Elizabeth Greenwald, Mitalee Christman, Lauren Penn, Nooshin Brinster, Tracey N Liebman
No abstract text is available yet for this article.
May 2018: JAAD Case Reports
https://www.readbyqxmd.com/read/29670775/mesenteric-panniculitis-presenting-as-fever-of-unknown-etiology-in-a-patient-with-history-of-abdominal-surgery
#9
Christopher P Irwin, Joo B Lee, Andrew Kim, Ijagha Eme, Christina Schofield, George Mount
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
https://www.readbyqxmd.com/read/29644775/exploring-the-combination-of-sski-and-topical-heparin-in-a-case-of-erythema-nodosum-migrans
#10
Manu Sehrawat, Niharika Dixit, Kabir Sardana, Purnima Malhotra
Erythema nodosum migrans (subacute nodular migratory panniculitis) is an uncommon type of panniculitis characterized by migrating subcutaneous nodules or plaque on the lower extremity. There are a very few cases of Erythema nodosum migrans reported and thus its appropriate treatment modality is not defined. We describe a case of a 30-year-old male with idiopathic erythema nodosum migrans which was manifest centrifugally spreading, slightly morpheaform erythematous plaque on the lower left leg. The patient was diagnosed initially and treated as a case of furunculosis with poor clinical response...
April 11, 2018: Dermatologic Therapy
https://www.readbyqxmd.com/read/29619994/geometric-alopecia-associated-with-lupus-erythematosus-panniculitis-of-the-scalp-a-case-series-of-nine-korean-patients
#11
Su-Kyung Park, Hyo-Hyun Yoo, Seok-Kweon Yun, Han-Uk Kim, Jin Park
No abstract text is available yet for this article.
April 5, 2018: European Journal of Dermatology: EJD
https://www.readbyqxmd.com/read/29618937/the-impact-of-alpha-1-antitrypsin-augmentation-therapy-on-neutrophil-driven-respiratory-disease-in-deficient-individuals
#12
REVIEW
Danielle M Dunlea, Laura T Fee, Thomas McEnery, Noel G McElvaney, Emer P Reeves
Alpha-1 antitrypsin (AAT) is the most abundant serine protease inhibitor circulating in the blood. AAT deficiency (AATD) is an autosomal codominant condition affecting an estimated 3.4 million individuals worldwide. The clinical disease associated with AATD can present in a number of ways including COPD, liver disease, panniculitis and antineutrophil cytoplasmic antibody vasculitis. AATD is the only proven genetic risk factor for the development of COPD, and deficient individuals who smoke are disposed to more aggressive disease...
2018: Journal of Inflammation Research
https://www.readbyqxmd.com/read/29610179/inherited-immunodeficiency-a-new-association-with-early-onset-childhood-panniculitis
#13
Brigitte Bader-Meunier, Frédéric Rieux-Laucat, Fabien Touzot, Marie-Louise Frémond, Isabelle André-Schmutz, Sylvie Fraitag, Christine Bodemer
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...
April 2018: Pediatrics
https://www.readbyqxmd.com/read/29594104/lymphocytic-lobular-panniculitis-a-diagnostic-challenge
#14
Silvia Alberti-Violetti, Emilio Berti
No abstract text is available yet for this article.
January 2018: Dermatopathology (Basel, Switzerland)
https://www.readbyqxmd.com/read/29592975/fulminant-hepatic-failure-in-the-setting-of-progressive-anca-associated-vasculitis-associated-with-a-rare-alpha-1-antitrypsin-phenotype-piee
#15
Ronald Reilkoff, Laurel Stephenson
Abnormalities in alpha-1 antitrypsin (AAT) proteins are risk factors for human disease. While the most common is AAT deficiency, a genetic disorder associated with chronic obstructive pulmonary disease, additional disorders associated with AAT abnormalities are increasingly recognised. We describe a middle-aged woman who presented with fulminant hepatic and multiorgan failure. Evaluation revealed the patient to have a rare AAT phenotype PiEE. Her clinical presentation was consistent with antineutrophilic cytoplasmic antibody-associated vasculitis, and her history suggested features of panniculitis...
March 28, 2018: BMJ Case Reports
https://www.readbyqxmd.com/read/29568849/intravascular-large-b-cell-lymphoma-presenting-as-panniculitis-clinically-a-case-report
#16
Yee Wei Phoon, Xuling Lin, T Thirumoorthy, Soo Yong Tan, Hwei Yee Lee, Soon Thye Lim, Haur Yueh Lee
No abstract text is available yet for this article.
March 2018: Singapore Medical Journal
https://www.readbyqxmd.com/read/29529121/panniculitis-pancreatitis-and-polyarthritis-a-rare-clinical-syndrome
#17
Paul M Graham, David A Altman, Stuart R Gildenberg
A rare triad composed of lobular panniculitis in the setting of pancreatitis and polyarthritis is termed panniculitis, pancreatitis, and polyarthritis (PPP) syndrome. Pancreatic panniculitis is a rare form of subcutaneous fat necrosis associated with underlying pancreatic disease. We describe a case of PPP syndrome and review the relevant literature associated with this rare clinical syndrome. Despite numerous adjuvant therapies, definitive treatment of PPP syndrome requires correction of the underlying pancreatic disease...
January 2018: Cutis; Cutaneous Medicine for the Practitioner
https://www.readbyqxmd.com/read/29527902/tender-red-subcutaneous-nodules-in-an-adult-female-a-challenging-diagnosis
#18
Juliana Moura Costa, Rita Seara Costa, Sofia Daniela Carvalho
Pancreatic panniculitis is an uncommon and rare skin complication of systemic fat necrosis associated with pancreatitis post-ampullectomy. Besides the rarity of the condition, the clinical history and physical examination for diagnosis is also important.
May 2018: Revista Española de Enfermedades Digestivas
https://www.readbyqxmd.com/read/29527901/pancreatic-panniculitis-as-a-presentation-symptom-of-acinar-cell-carcinoma
#19
Diego de Frutos Rosa, Laura Espinosa Taranilla, Pilar González de Canales de Simón, María Dolores Vélez Velázquez, Cristina Guirado Koch
Pancreatic panniculitis is a rare skin manifestation associated with pancreatic conditions. This condition has similar characteristics to those of other panniculitis types and its course parallels the triggering condition and may occasionally precede it. We report the case of a female patient with asymptomatic pancreatic panniculitis; the etiologic study identified a pancreatic acinar cell carcinoma with liver metastases.
May 2018: Revista Española de Enfermedades Digestivas
https://www.readbyqxmd.com/read/29524269/dermatomyositis-panniculitis-a-clinicopathological-and-immunohistochemical-study-of-18-cases
#20
A Santos-Briz, A Calle, K Linos, B Semans, A Carlson, O P Sangüeza, D Metze, L Cerroni, J L Díaz-Recuero, V Alegría-Landa, J M Mascaró, C Moreno, J L Rodríguez-Peralto, L Requena
BACKGROUND: Panniculitis occurring in dermatomyositis is uncommon, with only a few cases described in the literature, most of them as case reports. OBJECTIVE: This report describes the clinicopathological and immunohistochemical findings in a series of 18 patients with panniculitis associated with dermatomyositis. METHODS: In each patient, we collected the clinical data of the cutaneous lesions as well as the characteristic clinical and laboratory findings...
March 10, 2018: Journal of the European Academy of Dermatology and Venereology: JEADV
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