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*[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3].
*[Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3].
==Epidemiology and Demographics==
==Epidemiology and Demographics==
*This disorder is the second most common inflammatory disorder after familial mediterranean fever (FMF).
*The [[incidence]] of TNF receptor associated periodic syndrome is approximately 0.06 per 100,000 individuals of 16 years of age or younger worldwide.<ref name="LainkaNeudorf2009">{{cite journal|last1=Lainka|first1=E.|last2=Neudorf|first2=U.|last3=Lohse|first3=P.|last4=Timmann|first4=C.|last5=Stojanov|first5=S.|last6=Huss|first6=K.|last7=von Kries|first7=R.|last8=Niehues|first8=T.|title=Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics|journal=Rheumatology|volume=48|issue=8|year=2009|pages=987–991|issn=1462-0324|doi=10.1093/rheumatology/kep140}}</ref>
*The [[incidence]] of TNF receptor associated periodic syndrome is approximately 0.06 per 100,000 individuals of 16 years of age or younger worldwide.<ref name="LainkaNeudorf2009">{{cite journal|last1=Lainka|first1=E.|last2=Neudorf|first2=U.|last3=Lohse|first3=P.|last4=Timmann|first4=C.|last5=Stojanov|first5=S.|last6=Huss|first6=K.|last7=von Kries|first7=R.|last8=Niehues|first8=T.|title=Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics|journal=Rheumatology|volume=48|issue=8|year=2009|pages=987–991|issn=1462-0324|doi=10.1093/rheumatology/kep140}}</ref>
*TNF receptor associated periodic syndrome commonly affects individuals of 3 years of age. However, due to overlap of the symptoms with other [[disorders]] and possible misdiagnosis, it may be [[Diagnose|diagnosed]] in adolescence or adulthood. In addition, the variants with low penetrance tend to manifest later in the adult life.<ref name="CantariniIacoponi2011">{{cite journal|last1=Cantarini|first1=L.|last2=Iacoponi|first2=F.|last3=Lucherini|first3=O.M.|last4=Obici|first4=L.|last5=Brizi|first5=M.G.|last6=Cimaz|first6=R.|last7=Rigante|first7=D.|last8=Benucci|first8=M.|last9=Sebastiani|first9=G.D.|last10=Brucato|first10=A.|last11=Sabadini|first11=L.|last12=Simonini|first12=G.|last13=Giani|first13=T.|last14=Pasini|first14=F. Laghi|last15=Baldari|first15=C.T.|last16=Bellisai|first16=F.|last17=Valentini|first17=G.|last18=Bombardieri|first18=S.|last19=Paolazzi|first19=G|last20=Galeazzi|first20=M.|title=Validation of a Diagnostic Score for the Diagnosis of Autoinflammatory Diseases in Adults|journal=International Journal of Immunopathology and Pharmacology|volume=24|issue=3|year=2011|pages=695–702|issn=0394-6320|doi=10.1177/039463201102400315}}</ref>
*TNF receptor associated periodic syndrome commonly affects individuals of 3 years of age. However, due to overlap of the symptoms with other [[disorders]] and possible misdiagnosis, it may be [[Diagnose|diagnosed]] in adolescence or adulthood. In addition, the variants with low penetrance tend to manifest later in the adult life.<ref name="CantariniIacoponi2011">{{cite journal|last1=Cantarini|first1=L.|last2=Iacoponi|first2=F.|last3=Lucherini|first3=O.M.|last4=Obici|first4=L.|last5=Brizi|first5=M.G.|last6=Cimaz|first6=R.|last7=Rigante|first7=D.|last8=Benucci|first8=M.|last9=Sebastiani|first9=G.D.|last10=Brucato|first10=A.|last11=Sabadini|first11=L.|last12=Simonini|first12=G.|last13=Giani|first13=T.|last14=Pasini|first14=F. Laghi|last15=Baldari|first15=C.T.|last16=Bellisai|first16=F.|last17=Valentini|first17=G.|last18=Bombardieri|first18=S.|last19=Paolazzi|first19=G|last20=Galeazzi|first20=M.|title=Validation of a Diagnostic Score for the Diagnosis of Autoinflammatory Diseases in Adults|journal=International Journal of Immunopathology and Pharmacology|volume=24|issue=3|year=2011|pages=695–702|issn=0394-6320|doi=10.1177/039463201102400315}}</ref>
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*Cutaneous manifestations of TRAPS include an [[erythematous rash]] that overlies an area with [[myalgia]], erysiplas-like erythema, and [[urticaria]].
*Cutaneous manifestations of TRAPS include an [[erythematous rash]] that overlies an area with [[myalgia]], erysiplas-like erythema, and [[urticaria]].
*Eye involvement is characteristics for this [[disease]] among other [[Periodic fever syndrome|autoinflammatory diseases]] and may manifest with [[conjunctivitis]], [[periorbital edema]], and [[uveitis]].
*Eye involvement is characteristics for this [[disease]] among other [[Periodic fever syndrome|autoinflammatory diseases]] and may manifest with [[conjunctivitis]], [[periorbital edema]], and [[uveitis]].
*Signs consistent with acute abdomen may also be present.<ref name="ChenYu2014">{{cite journal|last1=Chen|first1=Yun-Ju|last2=Yu|first2=Hsin-Hui|last3=Yang|first3=Yao-Hsu|last4=Lau|first4=Yu-Lung|last5=Lee|first5=Wen-I|last6=Chiang|first6=Bor-Luen|title=Recurrent abdominal pain as the presentation of tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in an Asian girl: A case report and review of the literature|journal=Journal of Microbiology, Immunology and Infection|volume=47|issue=6|year=2014|pages=550–554|issn=16841182|doi=10.1016/j.jmii.2012.07.003}}</ref>
===Laboratory Findings===
===Laboratory Findings===
*An elevated concentration of blood acute phase reactants are observed both during and in between inflammatory attacks.<ref name="ChenYu2014">{{cite journal|last1=Chen|first1=Yun-Ju|last2=Yu|first2=Hsin-Hui|last3=Yang|first3=Yao-Hsu|last4=Lau|first4=Yu-Lung|last5=Lee|first5=Wen-I|last6=Chiang|first6=Bor-Luen|title=Recurrent abdominal pain as the presentation of tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in an Asian girl: A case report and review of the literature|journal=Journal of Microbiology, Immunology and Infection|volume=47|issue=6|year=2014|pages=550–554|issn=16841182|doi=10.1016/j.jmii.2012.07.003}}</ref>
*An elevated concentration of blood acute phase reactants are observed both during and in between inflammatory attacks.<ref name="ChenYu2014">{{cite journal|last1=Chen|first1=Yun-Ju|last2=Yu|first2=Hsin-Hui|last3=Yang|first3=Yao-Hsu|last4=Lau|first4=Yu-Lung|last5=Lee|first5=Wen-I|last6=Chiang|first6=Bor-Luen|title=Recurrent abdominal pain as the presentation of tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in an Asian girl: A case report and review of the literature|journal=Journal of Microbiology, Immunology and Infection|volume=47|issue=6|year=2014|pages=550–554|issn=16841182|doi=10.1016/j.jmii.2012.07.003}}</ref>
*An elevated level of serum TNF-α, C3, and C4 have also been reported.
===Electrocardiogram===
===Electrocardiogram===
*There are no [[ECG]] findings associated with TNF receptor-associated periodic syndrome.
*There are no [[ECG]] findings associated with TNF receptor-associated periodic syndrome.

Revision as of 15:24, 24 June 2019

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Synonyms and keywords: Tumor necrosis factor receptor-associated periodic syndrome (TRAPS); TRAPS; familial Hibernian fever; FHF; familial Caledonian fever

Overview

TNF receptor-associated periodic syndrome (also known as TRAPS or familial Hibernian fever) is a periodic fever syndrome associated with mutation in a receptor for the molecule tumor necrosis factor (TNF). Since this disease first described in Ireland, it was called Hibernian fever in reference to the ancient Latin name for Ireland, Hibernia.

Historical Perspective

  • TNF receptor-associated periodic syndrome was first described by Dr. Williamson in 1982 in an Irish-Scottish family affected by an autosomal dominant pattern disorder.[1]
  • The association between the TNFRSF1A gene locus and TNF receptor-associated periodic syndrome was made in 1998.[2]
  • In 2003, Dr. Weyhreter was the first to use etanercept (a fusion protein of the extracellular domain of TNFRSF1A and the Fc portion of IgG1) for the treatment of TRAPS, which results successful treatment of the patient.[3]

Classification

There is no established system for the classification of TNF receptor associated periodic syndrome.

Pathophysiology

  • TNF receptor associated periodic syndrome is an autosomal dominant inherited disorder due to mutation in the TNF Receptor Super Family 1A (TNFRSF1A) gene.[4]
  • Mutation in the gene is associated with abnormally structured TNF receptor which leads to impaired TNF-a binding and subsequent abnormal function of this factor in apoptosis and NF-κB pathway. However, the exact mechanisms causing febrile episodes remain to be cleared.[5][6][7]
  • Another hypothese is that mutation in the gene results in intracellular accumulation of the receptor. This abnormal accumulation of the receptor leads to an exaggerated inflammatory response to low levels of innate stimuli such as lipopolysaccharide (LPS).[8]

The main source of TNF is cells in the immune system called macrophages which produce it in response to infection and other stimuli. TNF helps activate other immune cells and plays a major role in the initiation of inflammation. Individuals with TRAPS have a mutation in the tumor necrosis factor receptor-1 (TNFR1) gene. The mechanisms by which mutations in TNFR1 lead to the TRAPS phenotype are still under investigation.

Differentiating ((Page name)) from Other Diseases

  • [Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as [differential dx1], [differential dx2], and [differential dx3].

Epidemiology and Demographics

  • This disorder is the second most common inflammatory disorder after familial mediterranean fever (FMF).
  • The incidence of TNF receptor associated periodic syndrome is approximately 0.06 per 100,000 individuals of 16 years of age or younger worldwide.[9]
  • TNF receptor associated periodic syndrome commonly affects individuals of 3 years of age. However, due to overlap of the symptoms with other disorders and possible misdiagnosis, it may be diagnosed in adolescence or adulthood. In addition, the variants with low penetrance tend to manifest later in the adult life.[10]
  • Although, first described in Ireland, this disorder has also been reported in other countries. However, it is especially common in Western countries rather than Asian countries.[11][12][13]

Risk Factors

  • There are no established risk factors for TNF receptor associated periodic syndrome. However, attacks may be triggered by factors such as:

Screening

There is insufficient evidence to recommend routine screening for TNF receptor associated periodic syndrome.

Natural History, Complications, and Prognosis

Diagnosis

Diagnostic Study of Choice

Presence Score
Periorbital oedema 21
Duration of episodes >6 days 19
Migratory rash 18
Myalgia 6
Reletavies affected 7
Absence Score
Vomiting 14
Aphthous stomatitis 15

History and Symptoms

Physical Examination

Common physical examination findings of TNF receptor-associated periodic syndrome include fever, skin rash, lymphadenopathy, and splenomegaly.[10]

Laboratory Findings

  • An elevated concentration of blood acute phase reactants are observed both during and in between inflammatory attacks.[13]
  • An elevated level of serum TNF-α, C3, and C4 have also been reported.

Electrocardiogram

  • There are no ECG findings associated with TNF receptor-associated periodic syndrome.

X-ray

  • There are no x-ray findings associated with TNF receptor-associated periodic syndrome.

Echocardiography or Ultrasound

CT scan

  • There are no CT scan findings associated with TNF receptor-associated periodic syndrome.
  • However, para-aortic and mesenteric lymphadenopathies have been reported in one case.[13]

MRI

  • There are no MRI findings associated with TNF receptor-associated periodic syndrome.

Other Imaging Findings

  • There are no other imaging findings associated with TNF receptor-associated periodic syndrome.

Other Diagnostic Studies

  • There are no other diagnostic studies associated with TNF receptor-associated periodic syndrome.

Treatment

Medical Therapy

  • Several medications have been studied for the treatment of TRAPS including high dose corticosteroids, etanercept, and infliximab.[13]
  • Response to the afromentioned treatment options reported to be different in different cases.

Surgery

  • Surgical intervention is not recommended for the management of TNF receptor-associated periodic syndrome.

Primary Prevention

  • There are no established measures for the primary prevention of TNF receptor-associated periodic syndrome.

Secondary Prevention

  • There are no established measures for the secondary prevention of TNF receptor-associated periodic syndrome.

References

  1. L. M. Williamson, D. Hull, R. Mehta, W. G. Reeves, B. H. Robinson & P. J. Toghill (1982). "Familial Hibernian fever". The Quarterly journal of medicine. 51 (204): 469–480. PMID 7156325.
  2. McDermott, Michael F.; Ogunkolade, B. William; McDermott, Elizabeth M.; Jones, Lisa C.; Wan, Ying; Quane, Kathleen A.; McCarthy, John; Phelan, Mark; Molloy, Michael G.; Powell, Richard J.; Amos, Christopher I.; Hitman, Graham A. (1998). "Linkage of Familial Hibernian Fever to Chromosome 12p13". The American Journal of Human Genetics. 62 (6): 1446–1451. doi:10.1086/301886. ISSN 0002-9297.
  3. Weyhreter, Heike; Schwartz, Marianne; Kristensen, Tim D.; Valerius, Niels H.; Paerregaard, Anders (2003). "A new mutation causing autosomal dominant periodic fever syndrome in a Danish family". The Journal of Pediatrics. 142 (2): 191–193. doi:10.1067/mpd.2003.15. ISSN 0022-3476.
  4. M. F. McDermott, I. Aksentijevich, J. Galon, E. M. McDermott, B. W. Ogunkolade, M. Centola, E. Mansfield, M. Gadina, L. Karenko, T. Pettersson, J. McCarthy, D. M. Frucht, M. Aringer, Y. Torosyan, A. M. Teppo, M. Wilson, H. M. Karaarslan, Y. Wan, I. Todd, G. Wood, R. Schlimgen, T. R. Kumarajeewa, S. M. Cooper, J. P. Vella, C. I. Amos, J. Mulley, K. A. Quane, M. G. Molloy, A. Ranki, R. J. Powell, G. A. Hitman, J. J. O'Shea & D. L. Kastner (1999). "Germline mutations in the extracellular domains of the 55 kDa TNF receptor, TNFR1, define a family of dominantly inherited autoinflammatory syndromes". Cell. 97 (1): 133–144. PMID 10199409. Unknown parameter |month= ignored (help)
  5. Nedjai, Belinda; Hitman, Graham A.; Yousaf, Nasim; Chernajovsky, Yuti; Stjernberg-Salmela, Susanna; Pettersson, Tom; Ranki, Annamari; Hawkins, Philip N.; Arkwright, Peter D.; McDermott, Michael F.; Turner, Mark D. (2008). "Abnormal tumor necrosis factor receptor I cell surface expression and NF-κB activation in tumor necrosis factor receptor–associated periodic syndrome". Arthritis & Rheumatism. 58 (1): 273–283. doi:10.1002/art.23123. ISSN 0004-3591.
  6. D'Osualdo, Andrea; Ferlito, Francesca; Prigione, Ignazia; Obici, Laura; Meini, Antonella; Zulian, Francesco; Pontillo, Alessandra; Corona, Fabrizia; Barcellona, Roberto; Duca, Marco Di; Santamaria, Giuseppe; Traverso, Francesco; Picco, Paolo; Baldi, Maurizia; Plebani, Alessandro; Ravazzolo, Roberto; Ceccherini, Isabella; Martini, Alberto; Gattorno, Marco (2006). "Neutrophils from patients withTNFRSF1A mutations display resistance to tumor necrosis factor–induced apoptosis: Pathogenetic and clinical implications". Arthritis & Rheumatism. 54 (3): 998–1008. doi:10.1002/art.21657. ISSN 0004-3591.
  7. Churchman, S M; Church, L D; Savic, S; Coulthard, L R; Hayward, B; Nedjai, B; Turner, M D; Mathews, R J; Baguley, E; Hitman, G A; Gooi, H C; Wood, P M D; Emery, P; McDermott, M F (2007). "A novel TNFRSF1A splice mutation associated with increased nuclear factor  appaB (NF- B) transcription factor activation in patients with tumour necrosis factor receptor associated periodic syndrome (TRAPS)". Annals of the Rheumatic Diseases. 67 (11): 1589–1595. doi:10.1136/ard.2007.078667. ISSN 0003-4967.
  8. Simon, A.; Park, H.; Maddipati, R.; Lobito, A. A.; Bulua, A. C.; Jackson, A. J.; Chae, J. J.; Ettinger, R.; de Koning, H. D.; Cruz, A. C.; Kastner, D. L.; Komarow, H.; Siegel, R. M. (2010). "Concerted action of wild-type and mutant TNF receptors enhances inflammation in TNF receptor 1-associated periodic fever syndrome". Proceedings of the National Academy of Sciences. 107 (21): 9801–9806. doi:10.1073/pnas.0914118107. ISSN 0027-8424.
  9. Lainka, E.; Neudorf, U.; Lohse, P.; Timmann, C.; Stojanov, S.; Huss, K.; von Kries, R.; Niehues, T. (2009). "Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics". Rheumatology. 48 (8): 987–991. doi:10.1093/rheumatology/kep140. ISSN 1462-0324.
  10. 10.0 10.1 10.2 Cantarini, L.; Iacoponi, F.; Lucherini, O.M.; Obici, L.; Brizi, M.G.; Cimaz, R.; Rigante, D.; Benucci, M.; Sebastiani, G.D.; Brucato, A.; Sabadini, L.; Simonini, G.; Giani, T.; Pasini, F. Laghi; Baldari, C.T.; Bellisai, F.; Valentini, G.; Bombardieri, S.; Paolazzi, G; Galeazzi, M. (2011). "Validation of a Diagnostic Score for the Diagnosis of Autoinflammatory Diseases in Adults". International Journal of Immunopathology and Pharmacology. 24 (3): 695–702. doi:10.1177/039463201102400315. ISSN 0394-6320.
  11. Aksentijevich, Ivona; Galon, Jérôme; Soares, Miguel; Mansfield, Elizabeth; Hull, Keith; Oh, Hye-Hyun; Goldbach-Mansky, Raphaela; Dean, Jane; Athreya, Balu; Reginato, Antonio J.; Henrickson, Michael; Pons-Estel, Bernardo; O’Shea, John J.; Kastner, Daniel L. (2001). "The Tumor-Necrosis-Factor Receptor–Associated Periodic Syndrome: New Mutations in TNFRSF1A, Ancestral Origins, Genotype-Phenotype Studies, and Evidence for Further Genetic Heterogeneity of Periodic Fevers". The American Journal of Human Genetics. 69 (2): 301–314. doi:10.1086/321976. ISSN 0002-9297.
  12. 12.0 12.1 Quintero, Javier; Saba, Jihan; Garcia, Carlos (2019). "Tumor Necrosis Factor Receptor-1 Associated Periodic Syndrome: Case Report and Review of an Auto-inflammatory Disorder". Cureus. doi:10.7759/cureus.3916. ISSN 2168-8184.
  13. 13.0 13.1 13.2 13.3 13.4 Chen, Yun-Ju; Yu, Hsin-Hui; Yang, Yao-Hsu; Lau, Yu-Lung; Lee, Wen-I; Chiang, Bor-Luen (2014). "Recurrent abdominal pain as the presentation of tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in an Asian girl: A case report and review of the literature". Journal of Microbiology, Immunology and Infection. 47 (6): 550–554. doi:10.1016/j.jmii.2012.07.003. ISSN 1684-1182.
  14. Federici, Silvia; Sormani, Maria Pia; Ozen, Seza; Lachmann, Helen J; Amaryan, Gayane; Woo, Patricia; Koné-Paut, Isabelle; Dewarrat, Natacha; Cantarini, Luca; Insalaco, Antonella; Uziel, Yosef; Rigante, Donato; Quartier, Pierre; Demirkaya, Erkan; Herlin, Troels; Meini, Antonella; Fabio, Giovanna; Kallinich, Tilmann; Martino, Silvana; Butbul, Aviel Yonatan; Olivieri, Alma; Kuemmerle-Deschner, Jasmin; Neven, Benedicte; Simon, Anna; Ozdogan, Huri; Touitou, Isabelle; Frenkel, Joost; Hofer, Michael; Martini, Alberto; Ruperto, Nicolino; Gattorno, Marco (2015). "Evidence-based provisional clinical classification criteria for autoinflammatory periodic fevers". Annals of the Rheumatic Diseases. 74 (5): 799–805. doi:10.1136/annrheumdis-2014-206580. ISSN 0003-4967.

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