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Page 1
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 autoinflammatory disorders a …
Schnitzler syndrome is a rare disorder characterized by a chronic urticarial rash associated with immunoglobulin M (IgM) monoclonal g …
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 syn …
Schnitzler syndrome is a very rare acquired systemic disease with many similarities to hereditary autoinflammatory syndromes. ...Othe …
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 autoinflammatory syndro …
The cytokine interleukin-1 (IL-1) plays a crucial role in the pathogenesis of the Schnitzler syndrome, and this explains the spectacu …
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 specialists …
Haematological malignancy and autoimmune conditions were among the top differentials, and she was eventually diagnosed with Schnitzler …
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 pain, a …
[Schnitzler's syndrome].
Henry B, Néel A, Barbarot S, Masseau A, Hamidou M. Henry B, et al. Rev Med Interne. 2013 Apr;34(4):224-9. doi: 10.1016/j.revmed.2012.08.004. Epub 2013 Jan 26. Rev Med Interne. 2013. PMID: 23357692 Review. French.
Schnitzler syndrome (SS) is a rare clinical entity, which belongs to the spectrum of monoclonal gammapathy-associated systemic disorders. ...
Schnitzler syndrome (SS) is a rare clinical entity, which belongs to the spectrum of monoclonal gammapathy-associated systemic disord …
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.
It is important to recognize Schnitzler syndrome for its remarkable response to interleukin (IL)-1 blockade. Besides, many cases of Schnitzler-like syndromes do not meet the diagnostic criteria of classical Schnitzler syndrome but display excellent response t …
It is important to recognize Schnitzler syndrome for its remarkable response to interleukin (IL)-1 blockade. Besides, many cases of …
[Schnitzler syndrome].
Ilbert C, Sabatiello M, Kurth W, Longrée L, Moutschen M, Darcis G. Ilbert C, et al. Rev Med Liege. 2020 Jul;75(7-8):553-557. Rev Med Liege. 2020. PMID: 32779911 Free article. French.
A treatment with colchicine was set up but the response to therapy was not satisfactory. The diagnosis of Schnitzler syndrome was eventually suggested based on the combination of monoclonal gammopathy, urticarial and pain. ...
A treatment with colchicine was set up but the response to therapy was not satisfactory. The diagnosis of Schnitzler syndrome was eve …
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. neutrophilic urt …
Schnitzler Syndrome is a rare acquired auto-inflammatory syndrome defined by an urticarial eruption and a monoclonal gammopathy, main …
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.
In addition to the abovementioned monogenic conditions, we describe Schnitzler's syndrome, a well-defined, acquired autoinflammatory condition without a clear genetic basis. ...
In addition to the abovementioned monogenic conditions, we describe Schnitzler's syndrome, a well-defined, acquired autoinflam …
2,800 results