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Schnitzler syndrome.
Gellrich FF, Günther C. Gellrich FF, et al. Dermatologie (Heidelb). 2025 Jun;76(Suppl 1):6-11. doi: 10.1007/s00105-019-4434-4. Dermatologie (Heidelb). 2025. 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: 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: 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.
Soubrier M. Soubrier M. Joint Bone Spine. 2008 May;75(3):263-6. doi: 10.1016/j.jbspin.2007.07.014. Epub 2008 Feb 22. Joint Bone Spine. 2008. PMID: 18378180 Review.
Schnitzler syndrome is characterized by monoclonal IgM gammopathy, urticaria, recurrent fever, evidence of inflammation, bone pain, and arthralgia, occasionally in combination with lymphadenopathy and/or hepatosplenomegaly. ...
Schnitzler syndrome is characterized by monoclonal IgM gammopathy, urticaria, recurrent fever, evidence of inflammation, bone …
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 …
A Modern Look at Schnitzler Syndrome - A Literature Review.
Kanabaj K, Bulińska B, Sokołowska-Wojdyło M. Kanabaj K, et al. Acta Dermatovenerol Croat. 2024 Nov;32(3):154-158. Acta Dermatovenerol Croat. 2024. PMID: 40654214 Review.
Schnitzler syndrome (SS) is an extremely rare acquired systemic disease that shares many similarities with various hereditary autoinflammatory syndromes. ...
Schnitzler syndrome (SS) is an extremely rare acquired systemic disease that shares many similarities with various hereditary …
Schnitzler syndrome without monoclonal gammopathy: a systematic review and case presentation.
Zhu C, Martinez-Jaramillo E, Ben-Shoshan M, Netchiporouk E, Chergui M, Fein M. Zhu C, et al. Clin Exp Dermatol. 2025 Dec 23;51(1):14-20. doi: 10.1093/ced/llaf403. Clin Exp Dermatol. 2025. PMID: 40971739 Free article.
Schnitzler syndrome (SS) is a rare autoinflammatory disorder that presents with chronic urticarial rash, neutrophilic urticarial dermatosis, monoclonal IgG or IgM gammopathy, recurrent fever, joint and/or bone pain and enlarged lymph nodes, spleen and/or liver. ...T …
Schnitzler syndrome (SS) is a rare autoinflammatory disorder that presents with chronic urticarial rash, neutrophilic urticari …
The Schnitzler syndrome.
Lipsker D. Lipsker D. Orphanet J Rare Dis. 2010 Dec 8;5:38. doi: 10.1186/1750-1172-5-38. Orphanet J Rare Dis. 2010. PMID: 21143856 Free PMC article. Review.
The Schnitzler syndrome is a rare and underdiagnosed entity which is considered today as being a paradigm of an acquired/late onset auto-inflammatory disease. ...It was exceedingly difficult to treat patients with this syndrome until the IL-1 receptor antagon …
The Schnitzler syndrome is a rare and underdiagnosed entity which is considered today as being a paradigm of an acquired/late …
[Schnitzler syndrome].
Gellrich FF, Günther C. Gellrich FF, et al. Hautarzt. 2018 Sep;69(9):761-772. doi: 10.1007/s00105-018-4250-2. Hautarzt. 2018. PMID: 30167710 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. …
557 results