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Panniculitis

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561. Bortezomib and Azacitidine in Treating Patients With Relapsed or Refractory T-Cell Lymphoma

belonging to one of the following WHO entities: Peripheral T-cell lymphoma, not otherwise specified (PTCL-NOS); Mycosis Fungoides and Sezary Syndrome (MF-SS); Angioimmunoblastic T-cell lymphoma (AITL); CD30-positive Anaplastic Large Cell Lymphoma (ALCL), systemic; T/NK-cell lymphoma, extranodal, nasal and nasal type; Hepatosplenic T-cell lymphoma, gamma/delta or alpha/beta; Enteropathy-associated T-cell lymphoma (EATL); Adult T-cell Leukemia/Lymphoma (ATLL); Subcutaneous panniculitis-like T-cell

2010 Clinical Trials

562. Protocol To Evaluate Patient Measurements After Ultrasonic Treatment

-up period, or has completed all other study-required follow-up less than 30 days before enrolment in this study. Keloid scars, hypertrophic scars or a history of abnormal healing. Thrombophlebitis. Bleeding or bruising disorders (e.g. idiopathic thrombocytopenic purpura, anticoagulated patients). Tissue ischemia in the area to be treated. Hypertension or abnormally high blood pressure. High cholesterol. Active collagen vascular disease (e.g. fibromyalgia, panniculitis, lupus etc.). Diabetes

2010 Clinical Trials

563. Panobinostat in Treating Patients With Relapsed or Refractory Non-Hodgkin Lymphoma

lymphoma; subcutaneous panniculitis-like T-cell lymphoma; angioimmunoblastic T-cell lymphoma; anaplastic large cell lymphoma - primary cutaneous type For lymphoplasmacytic lymphoma patients without measurable lymphadenopathy, measurable disease can be defined by both of the following criteria: bone marrow lymphoplasmacytosis with > 10% lymphoplasmacytic cells or aggregates, sheets, lymphocytes, plasma cells, or lymphoplasmacytic cells on bone marrow biopsy and quantitative IgM monoclonal protein

2010 Clinical Trials

564. Everolimus and Lenalidomide in Treating Patients With Relapsed or Refractory Non-Hodgkin or Hodgkin Lymphoma

fungoides/Sezary syndrome; Hodgkin Disease; Primary effusion lymphoma; Adult T-cell leukemia/lymphoma; Extranodal NK/T-cell lymphoma, nasal type; Enteropathy-type T-cell lymphoma; Hepatosplenic T-cell lymphoma; Subcutaneous panniculitis-like T-cell lymphoma; Angioimmunoblastic T-cell lymphoma; Anaplastic large cell lymphoma-primary cutaneous type; and Blastic plasmacytoid dendritic cell neoplasm Measurable disease by CT or MRI or PET/CT: Must have at least one lesion that has a single diameter of >= 2

2010 Clinical Trials

565. Prospective Study of Functional and Quality of Life Outcomes in Panniculectomy Patients

Panniculitis Procedure: panniculectomy Not Applicable Detailed Description: This is a prospective trial to determine what if any functional and quality of life benefits are achieved with a panniculectomy. Patients will be evaluated preoperatively and postoperatively with specific interventions aimed at describing their functional status. These interventions will include: echocardiogram, pulmonary function testing, arterial blood gas, functional capacity evaluation by physical therapy, and a quality of life (...) , 2018 Last Verified: August 2018 Layout table for additional information Studies a U.S. FDA-regulated Drug Product: No Studies a U.S. FDA-regulated Device Product: No Keywords provided by Wake Forest University Health Sciences ( Wake Forest University ): panniculitis panniculectomy Additional relevant MeSH terms: Layout table for MeSH terms Panniculitis Connective Tissue Diseases Skin Diseases

2010 Clinical Trials

566. Phase II, double-blinded, randomized study of enzastaurin plus pemetrexed as second-line therapy in patients with advanced non-small cell lung cancer. Full Text available with Trip Pro

) or overall survival (9.6 months in combination arm and 7.4 months in pemetrexed arm, p = 0.171). Drug-related serious adverse events included cerebrovascular accident, palpitations, and renal failure (n = 1, each) in combination arm and neutropenic sepsis, thrombocytopenia, and panniculitis (n = 1, each) in pemetrexed arm. Nonhematologic drug-related grade 3/4 toxicities were similar in both arms. Grade 3/4 hematologic toxicities were higher with the combination, specifically leukopenia (6.3% versus 0

2010 Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer Controlled trial quality: uncertain

567. Drug-induced skin pathology. Full Text available with Trip Pro

Drug-induced skin pathology. Drug-induced cutaneous rashes, whether confined to the skin or part of a systemic disease, are characterised by a spectrum of inflammatory disease patterns that include perivascular dermatitis, nodular and diffuse dermatitis, vesiculobullous lesions, pustular eruptions, sclerodermoid reactions, vasculitis, folliculitis/perifolliculitis and panniculitis. While a single drug can elicit a range of reaction patterns, no reaction pattern is specific for a particular drug

2009 Journal of Clinical Pathology

568. Silicone breast implant rupture presenting as bilateral leg nodules. (Abstract)

subcutaneous nodules on the medial aspect of the shins and ankles. Her medical history was notable for bilateral breast augmentation with silicone implants 30 years before presentation. Although there were no signs or symptoms on breast examination, ultrasonography and magnetic resonance imaging confirmed that both implants had ruptured. Histological examination of a punch biopsy from a nodule on the shin found lobular granulomatous panniculitis. An excisional biopsy of the lesion was analysed by scanning

2009 Clinical & Experimental Dermatology

569. Frequency, clinical features and prognosis of cutaneous manifestations in adult patients with reactive haemophagocytic syndrome. (Abstract)

patient had cytophagic histiocytic panniculitis. Histological features of maculopapular rash biopsies were usually nonspecific. The rate of in-hospital death was not significantly associated with cutaneous involvement.A generalized, nonpruriginous, transient, maculopapular rash is frequently observed in patients with RHS. Although nonspecific, awareness of this cutaneous involvement may assist physicians in the initial diagnosis of RHS.

2009 British Journal of Dermatology

570. Comparative analysis of subacute cutaneous lupus erythematosus and chronic cutaneous lupus erythematosus: clinical and immunological study of 270 patients. (Abstract)

of photosensitivity (P < 0.001), panniculitis (P = 0.009) and SLE (P = 0.003) than localized DLE. In patients with SCLE and those with CCLE, photosensitivity, arthralgias, arthritis, nephropathy and xerophthalmia were associated with SLE. In patients with SCLE, significant correlations existed between clinical and immunological data. Conclusions In our series, differences in the expression of CCLE and SCLE were found with respect to the distribution and type of lesions, systemic features and immunological

2009 British Journal of Dermatology

571. Aggressive subcutaneous panniculitis-like T-cell lymphoma with hemophagocytosis in two children (subcutaneous panniculitis-like T-cell lymphoma). (Abstract)

Aggressive subcutaneous panniculitis-like T-cell lymphoma with hemophagocytosis in two children (subcutaneous panniculitis-like T-cell lymphoma). Subcutaneous panniculitis-like T-cell lymphoma is an uncommon form of cutaneous lymphoma in the pediatric population. It is characterized histologically by subcutaneous infiltration of pleomorphic cytotoxic T cells, mimicking a lobular panniculitis. Although usually described as having an indolent clinical course, the condition may be complicated (...) by systemic involvement and hemophagocytic syndrome, resulting in a poorer prognosis. We present two pediatric patients with aggressive forms of subcutaneous panniculitis-like T-cell lymphoma complicated by hemophagocytic syndrome, and discuss the current literature.

2009 Journal of American Academy of Dermatology

572. Calcific panniculitis in adult-onset dermatomyositis. (Abstract)

Calcific panniculitis in adult-onset dermatomyositis. Dermatomyositis (DM) is an idiopathic inflammatory myopathy associated with characteristic cutaneous features. Panniculitis is a rarely reported clinical finding in this condition. This report describes two cases of adult-onset DM complicated by severe calcific panniculitis. In both cases, the associated pain and loss of function seemed to be best managed on combination anti-malarial therapy with mepacrine and hydroxychloroquine.

2009 Clinical & Experimental Dermatology

573. Relationship between abdominal trauma or surgery and mesenteric panniculitis Full Text available with Trip Pro

Relationship between abdominal trauma or surgery and mesenteric panniculitis Mesenteric panniculitis is a rare disease characterized by chronic non-specific inflammation of mesenteric fat tissue. Several etiologic and/or associated factors have been reported in the literature so far. Although trauma or surgery is one of the potential etiologic factors for mesenteric panniculitis, to the best of our knowledge, no strong correlation has been shown in the literature until now.

2009 World journal of gastroenterology : WJG

574. An Interesting Case of Recurrent Small Bowel Obstruction Full Text available with Trip Pro

An Interesting Case of Recurrent Small Bowel Obstruction Sclerosing mesenteritis is associated with a spectrum of diseases which include mesenteric lipodystrophy and mesenteric panniculitis. This inflammatory and fibrosing disorder can affect the small and large bowel wall and mesenteric vessels by exerting a mass effect. The following case highlights the difficulties with diagnosing and managing this unusual disease. A 64-year-old man presented with acute central abdominal pain, radiating

2009 Case reports in gastroenterology

575. Calciphylaxis in chronic renal failure: An approach to risk factors Full Text available with Trip Pro

Calciphylaxis in chronic renal failure: An approach to risk factors We present a case of calcifying panniculitis due to calciphylaxis in a nontherapy compliance 65-year-old man suffering from chronic renal failure. Calciphylaxis, a life threatening condition, is characterized by high calcium x phosphate product, presence of calcium crystals in the skin and secondary hyperparathyroidism. The clinical presentation includes painful firm plaques, which could progress to nonhealing ulcers. A review

2009 Indian Journal of Nephrology

576. Bortezomib and Romidepsin in Treating Patients With Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma, Indolent B-cell Lymphoma, Peripheral T-cell Lymphoma or Cutaneous T-Cell Lymphoma

associated lymphoid tissue (MALT)]) Lymphoplasmacytic lymphoma PTCL, relapsed or refractory: Anaplastic large cell lymphoma, anaplastic lymphoma kinase (ALK)-positive Anaplastic large cell lymphoma, ALK-negative Angioimmunoblastic T-cell lymphoma Enteropathy-associated T-cell lymphoma Extranodal natural killer (NK)/T-cell lymphoma, nasal type Hepatosplenic T-cell lymphoma PTCL, not otherwise specified (NOS) Subcutaneous panniculitis-like T-cell lymphoma CTCL: * CTCL with subtypes of mycosis fungoides

2009 Clinical Trials

577. The Effectiveness of Alemtuzumab Given in Combination With CHOP and ESHAP in Patients Newly Diagnosed With Peripheral T-Cell Lymphoma (PTCL)

to 65 Years (Child, Adult, Older Adult) Sexes Eligible for Study: All Accepts Healthy Volunteers: No Criteria Inclusion Criteria: Patients must have a diagnosis of one of the following histologic types according to the WHO classification: Angioimmunoblastic T-cell lymphoma Extranodal NK/T-cell lymphoma, nasal type Enteropathy-type T-cell lymphoma Hepatosplenic gamma-delta T-cell lymphoma Subcutaneous panniculitis-like T-cell lymphoma Anaplastic large-cell lymphoma, T/null cell, primary systemic type

2009 Clinical Trials

578. Panobinostat and Everolimus in Treating Patients With Recurrent Multiple Myeloma, Non-Hodgkin Lymphoma, or Hodgkin Lymphoma

Macroglobulinemia) CNS lymphoma Post transplant lymphoproliferative disorders Mycosis fungoides/Sezary syndrome Hodgkin Disease Primary effusion lymphoma Blastic natural killer (NK)-cell lymphoma Adult T-cell leukemia/lymphoma Extranodal NK/T-cell lymphoma, nasal type Enteropathy-type T-cell lymphoma Hepatosplenic T-cell lymphoma Subcutaneous panniculitis-like T-cell lymphoma Angioimmunoblastic T-cell lymphoma Anaplastic large cell lymphoma - primary cutaneous type For lymphoplasmacytic lymphoma patients

2009 Clinical Trials

579. EN (erythema nodosum)

EN (erythema nodosum) EN (erythema nodosum) - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search EN (erythema nodosum) Erythema nodosum is a panniculitis - an inflammation of the fat, seen principally in adult females. The female to male ratio is five to one but in children the ratio is 1:1 The disease can be seen at any age with a peak incidence between the ages of 20 and 30 years (1). The manifestation is with red nodules

2010 GP Notebook

580. erythema nodosum

erythema nodosum erythema nodosum - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search erythema nodosum Erythema nodosum is a panniculitis - an inflammation of the fat, seen principally in adult females. The female to male ratio is five to one but in children the ratio is 1:1 The disease can be seen at any age with a peak incidence between the ages of 20 and 30 years (1). The manifestation is with red nodules - in the literal

2010 GP Notebook

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