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Panniculitis

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641. Gnathostomiasis

, larvae invade the gastric wall and cause eosinophilia and various symptoms. Clinical features include: General: mild malaise, fever, urticaria, anorexia, nausea, vomiting, diarrhoea and epigastric pain. Skin: most commonly migratory, nodular panniculitis, [ ] soft tissue eruptions, boils and nodules in one or several areas. Pulmonary: cough, chest pain, dyspnoea or haemoptysis. Patient may cough up worm. Genitourinary: haematuria, urinary retention. Ophthalmological: decreased visual acuity

2008 Mentor

642. Erythema Induratum (Bazin's Disease)

to describe chronic inflammatory nodules of the legs that showed histopathological changes similar to those of erythema induratum, but without an association with TB. The vasculitis is of the larger vessels with panniculitis - an inflammation involving subcutaneous fat and occasionally muscle, with or without vasculitis. Erythema induratum and nodular vasculitis had been seen as the same disease for many years but nodular vasculitis is now considered to be a multifactorial syndrome of lobular panniculitis (...) second. Erythema induratum often remains undiagnosed or misdiagnosed because it can masquerade as other types of chronic nodules of the lower extremities. Differential diagnosis Cold panniculitis. . . . . . Lupus panniculitis. Investigations FBC and ESR. CXR. If a Mantoux test is performed it should be at a 1:10,000 dilution, as the response can be very marked. Unlike nodular vasculitis, erythema induratum is seen as a tuberculous disease and a strongly positive Mantoux response is regarded

2008 Mentor

643. Facial lupus erythematosus profundus in a 9-year-old boy. Full Text available with Trip Pro

Facial lupus erythematosus profundus in a 9-year-old boy. 9659310 1998 07 17 2018 11 13 0141-0768 91 4 1998 Apr Journal of the Royal Society of Medicine J R Soc Med Facial lupus erythematosus profundus in a 9-year-old boy. 207-8 Muncaster A A Selly Oak Hospital, Birmingham, UK. Stewart G G Moss C C Southwood T T eng Case Reports Journal Article England J R Soc Med 7802879 0141-0768 IM Child Facial Dermatoses diagnosis Humans Lymphatic Diseases etiology Male Panniculitis, Lupus Erythematosus

1998 Journal of the Royal Society of Medicine

644. Primary Cutaneous CD8-Positive Epidermotropic Cytotoxic T Cell Lymphomas : A Distinct Clinicopathological Entity with an Aggressive Clinical Behavior Full Text available with Trip Pro

of the 17 cases expressed markers characteristic of natural killer cells or gamma/delta T cells. Nine of 17 cases showed the characteristic clinical and histological features as well as clinical behavior of well defined types of CTCL, such as mycosis fungoides (2 cases), pagetoid reticulosis (2 cases), lymphomatoid papulosis (2 cases), and CD30+ large T cell lymphoma (2 cases), all of which usually express a CD4+ T cell phenotype, and 1 case of subcutaneous panniculitis-like T cell lymphoma. The other 8

1999 The American journal of pathology

645. Depsipeptide to Treat Patients With Cutaneous T-Cell Lymphoma and Peripheral T-Cell Lymphoma

will be enrolled in a fourth arm. These include but are not exclusively limited to: Enteropathy-type T cell lymphoma; Hepatosplenic T-cell lymphoma; Subcutaneous panniculitis-like T cell lymphoma; Angioimmunoblastic T-cell lymphoma; Anaplastic large cell lymphoma. Patients must have experienced disease progression after receiving prior standard treatment. There will be no limit on the number of prior regimens. Primitive T cell neoplasms and T cell leukemias will not be enrolled. Patients with peripheral T-cell

2000 Clinical Trials

646. Combination Chemotherapy With or Without Rituximab in Treating Older Patients With Non-Hodgkin's Lymphoma

marginal zone lymphoma (monocytoid) T-cell NHL including the following: Lymphoblastic precursor T-cell lymphoma Peripheral T-cell lymphoma (PTCL) not otherwise specified (NOS) Lennert's lymphoma T-zone lymphoma T-cell lymphoma of the angioimmunoblastic lymphadenopathy with dysproteinemia (AILD) type Anaplastic large cell lymphoma ALK^+ ALK^- Extranodal NK/T-cell lymphoma, nasal type Intestinal T/NK-cell lymphoma (with or without enteropathy) Hepatosplenic gamma-delta lymphoma Subcutaneous panniculitis

2003 Clinical Trials

647. Campath-1H and EPOCH to Treat Non-Hodgkin's T- and NK-Cell Lymphomas

(not otherwise specified (nos)), gamma-delta hepatosplenic T cell lymphoma, subcutaneous panniculitis-like T cell, NK-T cell lymphoma confirmed by pathology or flow cytometry staff of the Hematopathology Section, Laboratory of Pathology, NCI. Patients with alk-positive anaplastic large cell lymphoma and patients with T cell precursor disease are not eligible. Age greater than or equal to 17 years. Laboratory tests: Creatinine less than or equal to 1.5 mg/dL or creatinine clearance greater than or equal to 60

2003 Clinical Trials

648. Defect of a complement receptor 3 epitope in a patient with systemic lupus erythematosus. Full Text available with Trip Pro

Defect of a complement receptor 3 epitope in a patient with systemic lupus erythematosus. Complement receptor 3 (CR3) is expressed on cells of the reticuloendothelial system and involved in the clearance of immune complexes. In this article a patient with a deficiency of the C3bi binding site of this receptor is described. Clinically this patient exhibited predominantly cutaneous manifestations of a systemic lupus erythematosus with an immune vasculitis and panniculitis. The deficiency

1993 Journal of Clinical Investigation

649. Out of Africa: observations on the histopathology of Mycobacterium ulcerans infection. Full Text available with Trip Pro

Panniculitis microbiology pathology Skin pathology Skin Diseases, Bacterial microbiology pathology Skin Ulcer microbiology pathology 20 1993 1 1 1993 1 1 0 1 1993 1 1 0 0 ppublish 8432888 PMC501092 Trop Geogr Med. 1959 Dec;11:293-312 14406764 Int J Lepr. 1965 Jul-Sep;33(3):Suppl:698-709 5322711 Int J Lepr Other Mycobact Dis. 1966 Jul-Sep;34(3):255-73 5950347 Med J Aust. 1967 Mar 4;1(9):427-31 5336860 Australas J Dermatol. 1985 Aug;26(2):67-73 4084161 East Afr Med J. 1963 Apr;40:113-7 13931729 J Trop Med

1993 Journal of Clinical Pathology

650. Cutaneous lymphomas with prominent granulomatous reaction: a potential pitfall in the histopathologic diagnosis of cutaneous T- and B-cell lymphomas. (Abstract)

cutaneous T-cell lymphomas and B-cell lymphomas (primary cutaneous lymphoma 22, secondary cutaneous lymphoma one). Biopsies of 23 patients with histopathologic features of cutaneous T-cell lymphoma or cutaneous B-cell lymphoma with prominent granulomatous reaction were included in this study. A prominent granulomatous reaction was defined as the presence of a granulomatous component exceeding 25% of the dermal infiltrate. There were 14 cases of mycosis fungoides, two of subcutaneous panniculitis-like T

2002 American Journal of Surgical Pathology

651. Cytotoxic/natural killer cell cutaneous lymphomas. Report of EORTC Cutaneous Lymphoma Task Force Workshop. (Abstract)

collected for a workshop of the European Organization for Research and Treatment of Cancer Cutaneous Lymphoma Task Force, to better clarify the clinical, morphologic, and phenotypic features of these uncommon tumors.Several categories with different clinical and pathologic features were delineated: 1) aggressive, CD8+, epidermotropic, cytotoxic T-cell lymphoma; 2) mycosis fungoides, cytotoxic immunophenotype variant; 3) subcutaneous panniculitis-like T-cell lymphoma; 4) NK/T-cell lymphoma, nasal type; 5

2003 Cancer

652. Sporotrichoid cutaneous Mycobacterium avium complex infection. (Abstract)

ulcers, inflammatory nodules, panniculitis, pustular lesions, and draining sinuses. Localized skin involvement resembling sporotrichosis is unusual and to our knowledge has been reported only once in the English-language literature. We describe an additional case of primary cutaneous M avium complex infection manifesting as sporotrichosis-like lesions on a patient with AIDS.

2002 Journal of American Academy of Dermatology

653. Branched filaments no fungus, ovoid bodies no bacteria: Two unusual cases of mycetoma. (Abstract)

Branched filaments no fungus, ovoid bodies no bacteria: Two unusual cases of mycetoma. We describe a 58-year-old man presenting with necrotizing panniculitis of the lower right leg and a 64-year-old woman with a clinically similar lesion combined with pustular eruptions and subsequent ulceration on the forehead. In the first patient, Giemsa staining showed small ovoid bodies and Grocott staining revealed hyphae. Histology from the process on the forehead showed branched filaments

2003 Journal of American Academy of Dermatology

654. Characteristics of cutaneous lymphomas in Korea. (Abstract)

a recent 3-year period. The clinical records, haematoxylin & eosin-stained slides and immunohistochemical stains from 80 patients with malignant lymphomas of the skin were reviewed. In our study, the most frequent cutaneous lymphoma was mycosis fungoides. Compared with Western countries, Korea had higher rates of NK/T cell lymphoma and subcutaneous panniculitis-like T-cell lymphoma and a much lower rate of B-cell lymphoma. The occurrence rates for various subtypes of malignant lymphoma in Korea

2003 Clinical & Experimental Dermatology

655. Cutaneous lymphomas other than mycosis fungoides in Singapore: a clinicopathological analysis using recent classification systems. (Abstract)

. The immunohistological diagnosis was correlated with the clinical presentation and staging investigations for the final diagnosis and the course of disease recorded.Non-MF T-cell lymphomas presenting in the skin comprised 31 cases (78%) and were 3(1/2) times more common than B-cell lymphomas, which comprised nine cases (22%). The common subtypes were lymphomatoid papulosis, CD30+ large cell cutaneous T-cell lymphoma and subcutaneous panniculitis-like T-cell lymphoma. The commonly ascribed B-cell pattern (...) with infiltrates in the mid and deep dermis and perivascular spaces was seen in 60% of T-cell lymphomas. Overall, there were equal numbers of primary cutaneous T-cell lymphomas and those due to concurrent or secondary cutaneous lymphoma. Five of six cases of subcutaneous panniculitis-like T-cell lymphoma had concurrent cutaneous and systemic involvement and their median survival was 7 months.The predominance of cutaneous T-cell lymphomas in this case series closely matched that reported from east Asia

2003 British Journal of Dermatology

656. The spectrum of cutaneous disease in multiple myeloma. (Abstract)

of lymphocyte recovery (3), thrombocytopenia-related lesions (9), normolipemic plane xanthoma (1), amyloidosis (1), Sweet's syndrome (7), panniculitis (1), papulosquamous lesions (18), bullous diseases (17), vasculitis (11), infectious lesions (41), granulomatous dermatitis (6), alopecia cicatrisata (1), nonspecific lesions (77), and unrelated lesions (2).Skin biopsy specimens from patients with MM less than 60 days from transplant most commonly show sequelae of the transplant such as graft-versus-host

2003 Journal of American Academy of Dermatology

657. panniculitis

panniculitis panniculitis - General Practice Notebook This site is intended for healthcare professionals General Practice Notebook | Medical search panniculitis 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 translation

2010 GP Notebook

658. Panniculitis and lipoatrophy after subcutaneous injection of interferon β‐1b in a patient with multiple sclerosis Full Text available with Trip Pro

Panniculitis and lipoatrophy after subcutaneous injection of interferon β‐1b in a patient with multiple sclerosis 16782776 2006 12 04 2018 11 13 1468-330X 77 12 2006 Dec Journal of neurology, neurosurgery, and psychiatry J. Neurol. Neurosurg. Psychiatry Panniculitis and lipoatrophy after subcutaneous injection of interferon beta-1b in a patient with multiple sclerosis. 1382-3 O'Sullivan S S SS Cronin E M EM Sweeney B J BJ Bourke J F JF Fitzgibbon J J eng Case Reports Letter 2006 06 16 (...) England J Neurol Neurosurg Psychiatry 2985191R 0022-3050 0 Adjuvants, Immunologic 0 Recombinant Proteins 145155-23-3 Interferon beta-1b 77238-31-4 Interferon-beta IM Adipose Tissue pathology Adjuvants, Immunologic adverse effects therapeutic use Adult Atrophy chemically induced Humans Interferon beta-1b Interferon-beta adverse effects therapeutic use Male Multiple Sclerosis drug therapy Panniculitis chemically induced Recombinant Proteins 2006 6 20 9 0 2006 12 9 9 0 2006 6 20 9 0 ppublish 16782776

2006 Journal of neurology, neurosurgery, and psychiatry

659. An Unusual Presentation of Mesenteric Panniculitis Full Text available with Trip Pro

An Unusual Presentation of Mesenteric Panniculitis 19061011 2009 08 21 2018 11 13 1980-5322 63 6 2008 Dec Clinics (Sao Paulo, Brazil) Clinics (Sao Paulo) An unusual presentation of mesenteric panniculitis. 843-4 S1807-59322008000600023 Ferrari Teresa Cristina A TC Couto Carolina M CM Vilaça Tatiane S TS Xavier Marcelo A P MA Faria Luciana C LC eng Case Reports Letter Brazil Clinics (Sao Paulo) 101244734 1807-5932 0 Anti-Inflammatory Agents VB0R961HZT Prednisone IM Adult Anti-Inflammatory Agents (...) therapeutic use Humans Male Panniculitis, Peritoneal diagnosis drug therapy pathology Prednisone therapeutic use 2008 12 9 9 0 2009 8 22 9 0 2008 12 9 9 0 ppublish 19061011 S1807-59322008000600023 PMC2664289 Radiographics. 2003 Nov-Dec;23(6):1561-7 14615565 Gastroenterology. 1980 Aug;79(2):352-6 7399242 Am J Surg Pathol. 1989 Jun;13(6):513-21 2658633 Clin Gastroenterol Hepatol. 2007 May;5(5):589-96; quiz 523-4 17478346 Ann Chir. 2006 Feb;131(2):85-90 16242659 Rev Med Interne. 2007 May;28(5):289-95

2008 Clinics (Sao Paulo, Brazil)

660. Cytophagic histiocytic panniculitis with fatal haemophagocytic lymphohistiocytosis in a paediatric patient with perforin gene mutation Full Text available with Trip Pro

Cytophagic histiocytic panniculitis with fatal haemophagocytic lymphohistiocytosis in a paediatric patient with perforin gene mutation 17601962 2008 06 06 2018 11 13 0021-9746 60 10 2007 Oct Journal of clinical pathology J. Clin. Pathol. Cytophagic histiocytic panniculitis with fatal haemophagocytic lymphohistiocytosis in a paediatric patient with perforin gene mutation. 1168-9 Chen Rong-Long RL Division of Paediatric Hematology/Oncology, Cancer Centre, Chi-Mei Medical Centre, Liou Ying Campus (...) , Tainan, Taiwan. Hsu Yung-Hsiang YH Ueda Ikuyo I Imashuku Shinsaku S Takeuchi Kengo K Tu Benjamin Pang-hsien BP Chuang Shih-Sung SS eng Case Reports Journal Article 2007 06 29 England J Clin Pathol 0376601 0021-9746 126465-35-8 Perforin AIM IM Base Sequence Child Fatal Outcome Female Humans Lymphohistiocytosis, Hemophagocytic genetics pathology Molecular Sequence Data Panniculitis genetics pathology Perforin genetics Point Mutation 2007 7 3 9 0 2008 6 7 9 0 2007 7 3 9 0 ppublish 17601962 jcp

2007 Journal of Clinical Pathology

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