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Dermatomyositis: nailfold capillaroscopy patterns and a general survey.
Acta Dermatovenerol Alp Pannonica Adriat
June 2024
Jean Françoise Merlen Research Center of Vascular Diseases, Frosinone, Italy.
Introduction: Dermatomyositis (DM) is a group of autoimmune idiopathic inflammatory myopathies characterized by typical cutaneous signs and symptoms of muscle involvement. The diseases can be associated with cancer in the paraneoplastic syndrome, calcinosis, interstitial lung disease, other autoimmune connective tissue diseases (in overlap syndrome), and Raynaud's phenomenon.
Methods: Clinical and capillaroscopic data were gathered from 43 patients with DM.
Digital Gangrene as a Paraneoplastic Manifestation of Peripheral T-cell Lymphoma Not Otherwise Specified Type.
J Assoc Physicians India
January 2024
Consultant Hematopathologist, GKNM Hospital, Coimbatore, Tamil Nadu, India.
Background: Peripheral T cell lymphoma (PTCL), not otherwise specified (NOS) is a heterogenous group of predominantly nodal T cell lymphomas that generally presents with lymphadenopathy with or without extra nodal involvement. Acral vascular syndrome clinically presents as digital ischemia with Raynaud's phenomenon and acral cyanosis. Although, this condition is commonly associated with connective tissue disorder, smoking and vasculitis, its association with lymphoid malignancy is very rare.
View Article and Find Full Text PDFPainful Raynaud's mimics.
Best Pract Res Clin Rheumatol
March 2024
Department of Internal Medicine, Division of Rheumatology, University of Michigan, 300 North Ingalls Building - Rm 7C27, Ann Arbor, MI, 48109, USA. Electronic address:
Article Synopsis
- Raynaud's syndrome is commonly associated with autoimmune diseases and requires proper diagnosis to differentiate it from other similar conditions.
- Distinguishing painful Raynaud's mimickers is crucial because they can increase patient stress and lead to unnecessary medical procedures.
- The review aims to educate on Raynaud's syndrome, identify painful mimickers, and provide updated recommendations for diagnosis and management.
Nonbacterial thrombotic endocarditis of mitral valve associated with a lymphoproliferative malignancy: case report and literature review.
Cardiooncology
April 2024
Hematology Department, Hospital of Divino Espírito Santo of Ponta Delgada, São Miguel Island, Azores, Portugal.
Background: Non-bacterial thrombotic endocarditis (NBTE) is a rare condition marked by sterile vegetations on cardiac valves, often linked to rheumatologic diseases, autoimmune disorders, and advanced solid malignancies. An early diagnosis and treatment of the associated clinical condition are mandatory, although they do not usually eliminate valvular vegetations, making anticoagulation essential to prevent embolic events. Despite variability, the prognosis of NBTE is usually unfavorable due to recurrent embolic events and the severity of the primary condition, typically advanced cancer.
View Article and Find Full Text PDFAssociation between systemic sclerosis, palmar fasciitis with polyarthritis, Raynaud's phenomenon and erythromelalgia with underlying malignancy.
Reumatologia
September 2022
Musgrave Park Hospital, Belfast, United Kingdom.
The symptoms of a rheumatic disease may also be a sign of a proliferative process. These include conditions that present with skin and vascular changes such as systemic sclerosis and Raynaud's phenomenon with peripheral ischaemia and ulceration. Furthermore, the less common conditions - erythromelalgia or palmar fasciitis with polyarthritis may also accompany cancer.
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