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Schnitzler syndrome.
Gellrich FF, Günther C. Gellrich FF, et al. Hautarzt. 2019 Jun 5. doi: 10.1007/s00105-019-4434-4. Online ahead of print. Hautarzt. 2019. PMID: 31165908 Review. English.
Schnitzler syndrome is a very rare acquired systemic disease with many similarities to hereditary autoinflammatory syndromes. ...Other clinical features include fever, muscle, bone, and/or joint pain, and lymphadenopathy. About 15-20% of patients with Schnitzler …
Schnitzler syndrome is a very rare acquired systemic disease with many similarities to hereditary autoinflammatory syndromes. …
Schnitzler Syndrome: a Review.
Gusdorf L, Lipsker D. Gusdorf L, et al. Curr Rheumatol Rep. 2017 Aug;19(8):46. doi: 10.1007/s11926-017-0673-5. Curr Rheumatol Rep. 2017. PMID: 28718061 Review.
The cytokine interleukin-1 (IL-1) plays a crucial role in the pathogenesis of the Schnitzler syndrome, and this explains the spectacular efficiency of IL-1 blocking therapies. The Schnitzler syndrome is now considered as a late-onset acquired autoinfla …
The cytokine interleukin-1 (IL-1) plays a crucial role in the pathogenesis of the Schnitzler syndrome, and this explains the s …
Schnitzler Syndrome: Insights into Its Pathogenesis, Clinical Manifestations, and Current Management.
Braud A, Lipsker D. Braud A, et al. Biomolecules. 2024 May 31;14(6):646. doi: 10.3390/biom14060646. Biomolecules. 2024. PMID: 38927050 Free PMC article. Review.
Schnitzler syndrome is a rare disorder characterized by a chronic urticarial rash associated with immunoglobulin M (IgM) monoclonal gammopathy. Schnitzler syndrome shares strong clinicopathologic similarities with monogenic IL-1-mediated autoinflammato …
Schnitzler syndrome is a rare disorder characterized by a chronic urticarial rash associated with immunoglobulin M (IgM) monoc …
Schnitzler syndrome.
Sankar PR, Janamanchi V, Vondenberg J, Calabrese C. Sankar PR, et al. BMJ Case Rep. 2023 May 18;16(5):e254334. doi: 10.1136/bcr-2022-254334. BMJ Case Rep. 2023. PMID: 37202108 Free PMC article.
Haematological malignancy and autoimmune conditions were among the top differentials, and she was eventually diagnosed with Schnitzler syndrome. A multidisciplinary team consisting of internal medicine, rheumatology, infectious disease and haematology-oncology speci …
Haematological malignancy and autoimmune conditions were among the top differentials, and she was eventually diagnosed with Schnitzler …
Schnitzler Syndrome: the paradigm of an acquired adult-onset auto-inflammatory disease.
Gusdorf L, Lipsker D. Gusdorf L, et al. G Ital Dermatol Venereol. 2020 Oct;155(5):567-573. doi: 10.23736/S0392-0488.20.06692-4. G Ital Dermatol Venereol. 2020. PMID: 33295738 Review.
Schnitzler Syndrome is a rare acquired auto-inflammatory syndrome defined by an urticarial eruption and a monoclonal gammopathy, mainly of the IgM kappa isotype. ...Hence, recurrent fever, urticarial rash with a neutrophilic infiltrate on skin biopsy (i.e. ne …
Schnitzler Syndrome is a rare acquired auto-inflammatory syndrome defined by an urticarial eruption and a monoclonal ga …
Schnitzler syndrome and Schnitzler-like syndromes.
Chu CQ. Chu CQ. Chin Med J (Engl). 2022 May 20;135(10):1190-1202. doi: 10.1097/CM9.0000000000002015. Chin Med J (Engl). 2022. PMID: 35089885 Free PMC article.
Schnitzler syndrome is often underdiagnosed. Patients with Schnitzler syndrome may present to dermatologists and allergists for urticaria, hematologists for MGUS, or rheumatologists for arthritis. It is important to recognize Schnitzler syndr …
Schnitzler syndrome is often underdiagnosed. Patients with Schnitzler syndrome may present to dermatologists and …
[Schnitzler syndrome].
Gellrich FF, Günther C. Gellrich FF, et al. Z Rheumatol. 2019 Feb;78(1):43-54. doi: 10.1007/s00393-019-0591-1. Z Rheumatol. 2019. PMID: 30666414 German.
Schnitzler syndrome is a very rare acquired systemic disease with many similarities to hereditary autoinflammatory syndromes. ...Other clinical features include fever, muscle, bone and/or joint pain, and lymphadenopathy. About 15-20% of patients with Schnitzler …
Schnitzler syndrome is a very rare acquired systemic disease with many similarities to hereditary autoinflammatory syndromes. …
Hereditary systemic autoinflammatory diseases and Schnitzler's syndrome.
Kacar M, Pathak S, Savic S. Kacar M, et al. Rheumatology (Oxford). 2019 Nov 1;58(Suppl 6):vi31-vi43. doi: 10.1093/rheumatology/kez448. Rheumatology (Oxford). 2019. PMID: 31769858 Free PMC article. Review.
Hereditary fever syndromes, such as FMF, TNF receptor-associated periodic syndrome, cryopyrin-associated periodic syndromes and mevalonate kinase deficiency, were the first group of systemic autoinflammatory diseases for which a genetic basis was established, between 1999 …
Hereditary fever syndromes, such as FMF, TNF receptor-associated periodic syndrome, cryopyrin-associated periodic syndromes and meval …
Schnitzler Syndrome.
Badawi AH, Gierer S, Fraga GR. Badawi AH, et al. Allergy Asthma Proc. 2014 Jan-Feb;35(1):75-7. doi: 10.2500/aap.2014.35.3703. Allergy Asthma Proc. 2014. PMID: 24433601
A 48-year-old man with typical features of Schnitzler Syndrome is presented, followed by a discussion of the pathogenesis and clinical aspects of this rare disease. ...Clinical pearls and pitfalls are emphasized to aid clinicians from varying specialties in recogniz …
A 48-year-old man with typical features of Schnitzler Syndrome is presented, followed by a discussion of the pathogenesis and …
Schnitzler syndrome.
Gallo J, Paira S. Gallo J, et al. Reumatol Clin. 2015 Mar-Apr;11(2):124-5. doi: 10.1016/j.reuma.2014.07.002. Epub 2014 Nov 22. Reumatol Clin. 2015. PMID: 25441494 Free article. English, Spanish. No abstract available.
517 results

Searches related to "schnitzler syndrome"