Eosinophilic fasciitis
| Eosinophilic fasciitis | |
|---|---|
| Classification and external resources | |
| Specialty | rheumatology |
| ICD-10 | M35.4 |
| ICD-9-CM | 728.89 |
| OMIM | 226350 |
| DiseasesDB | 29427 |
| MedlinePlus | 000447 |
| eMedicine | med/686 |
Eosinophilic fasciitis (/ˌiːəˌsɪnəˈfɪlɪk ˌfæʃiˈaɪtᵻs, ˌiːoʊ-, -ˌfæsi-/[1][2]), also known as "Shulman's syndrome",[3] is a form of fasciitis, the inflammatory diseases that affect the fascia, the connective tissues surrounding muscles, blood vessels and nerves. Unlike other diseases in that category, it is limited to the arms and legs, and usually resolves itself, although some cases require corticosteroids, and some cases are associated with aplastic anemia.[4]
The presentation of eosinophilic fasciitis is similar to scleroderma or systemic sclerosis. However, unlike scleroderma, it affects the fascia, not the skin (dermis). The characteristic and severe effects of scleroderma and systemic sclerosis, such as Raynaud's syndrome, involvement of the extremities, prominent small blood vessels (telangiectasia), and visceral changes such as swallowing problems, are absent.
It was first characterized in 1974,[5] and it is not yet known whether it is actually a distinct condition or just a different presentation. However, it remains used for diagnostic purposes.
Several cases have been reported after strenuous exercise.
Symptoms
As it is a rare disease, a clear set of symptoms is difficult to define. Usually, patients show severe pain and swelling is reported but clinical presentations vary. It can have an 'orange peel' like appearance.[6] Less common features are joint pain and carpal tunnel syndrome.
Treatment
Common treatments include corticosteroids[7] such as prednisone, though other medications such as hydroxychloroquine[8] have also been used. The prognosis is usually good in the case of an early treatment if there is no visceral involvement.[6][9]
Diagnosis
The key to diagnosis is skin changes combined with blood eosinophilia but the most accurate test is a skin, fascia and muscle biopsy.
Epidemiology
Typical age of onset is around 40 to 50 years. It is not clear whether it is more common in women than men - patient numbers are small and some studies report a preponderance of men and others women.[10] It is also found in children.
See also
References
- ↑ "Eosinophilic". Oxford Dictionaries. Oxford University Press. Retrieved 2016-01-21. "fasciitis". Oxford Dictionaries. Oxford University Press. Retrieved 2016-01-21.
- ↑ "Eosinophilic". Merriam-Webster Dictionary. Retrieved 2016-01-21. "fasciitis". Merriam-Webster Dictionary. Retrieved 2016-01-21.
- ↑ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 1-4160-2999-0.
- ↑ Merck Manual, Professional Edition, Eosinophilic Fasciitis
- ↑ Shulman LE (1975). "Diffuse fasciitis with eosinophilia: a new syndrome?". Trans. Assoc. Am. Physicians. 88: 70–86. PMID 1224441.
- 1 2 Bischoff, Lindsay; Chris T. Derk (January 2008). "Eosinophilic fasciitis: demographics, disease pattern and response to treatment: report of 12 cases and review of the literature". International Journal of Dermatology. 47 (1): 29–35. doi:10.1111/j.1365-4632.2007.03544.x. PMID 18173597.
- ↑ Antic M, Lautenschlager S, Itin PH (2006). "Eosinophilic fasciitis 30 years after - what do we really know? Report of 11 patients and review of the literature". Dermatology (Basel). 213 (2): 93–101. doi:10.1159/000093847. PMID 16902285.
- ↑ Lakhanpal S, Ginsburg WW, Michet CJ, Doyle JA, Moore SB (1988). "Eosinophilic fasciitis: clinical spectrum and therapeutic response in 52 cases". Semin. Arthritis Rheum. 17 (4): 221–31. doi:10.1016/0049-0172(88)90008-X. PMID 3232080.
- ↑ Valadares, Diana; Joao Neves; Isabel Almeida; Carlos Lopes; Carlos Vasconcelos (February 2011). "Iron Lady: A Case of Eosinophilic Fasciitis". Journal of Medical Case Reports. 2: 34–36. doi:10.4021/jmc118w.
- ↑ Wojas-Pelc A, Wielowieyska-Szybińska D, Lipko-Godlewska S (2004). "[Eosinophilic fasciitis--current database]". Pol. Merkur. Lekarski (in Polish). 16 (96): 585–8. PMID 15510903.
Further reading
- Lakhanpal, Sharad; Ginsburg, William W.; Michet, Clement J.; Doyle, John A.; Moore, S.Breanndan (1988). "Eosinophilic fasciitis: Clinical spectrum and therapeutic response in 52 cases". Seminars in Arthritis and Rheumatism. 17 (4): 221–231. doi:10.1016/0049-0172(88)90008-X. ISSN 0049-0172. PMID 3232080.
- Barnes L, Rodnan GP, Medsger TA, Short D (August 1979). "Eosinophilic fasciitis. A pathologic study of twenty cases". The American Journal of Pathology. 96 (2): 493–518. PMC 2042453
. PMID 474708. - Doyle JA, Ginsburg WW (September 1989). "Eosinophilic fasciitis". The Medical Clinics of North America. 73 (5): 1157–66. PMID 2671538.
- Michet CJ, Doyle JA, Ginsburg WW (January 1981). "Eosinophilic fasciitis: report of 15 cases". Mayo Clinic Proceedings. Mayo Clinic. 56 (1): 27–34. PMID 7453247.
- Bennett, R M; Herron, A; Keogh, L (1977). "Eosinophilic fasciitis. Case report and review of the literature.". Annals of the Rheumatic Diseases. 36 (4): 354–359. doi:10.1136/ard.36.4.354. ISSN 0003-4967.
- Falanga, Vincent; Medsger, Thomas A. (1987). "Frequency, levels, and significance of blood eosinophilia in systemic sclerosis, localized scleroderma, and eosinophilic fasciitis". Journal of the American Academy of Dermatology. 17 (4): 648–656. doi:10.1016/S0190-9622(87)70251-5. ISSN 0190-9622.
- Varga J, Kähäri VM (November 1997). "Eosinophilia-myalgia syndrome, eosinophilic fasciitis, and related fibrosing disorders". Current Opinion in Rheumatology. 9 (6): 562–70. doi:10.1097/00002281-199711000-00013. PMID 9375286.
- Kent, Lawrence T.; Cramer, Stewart F.; Moskowitz, Roland W. (1981). "Eosinophilic fasciitis". Arthritis & Rheumatism. 24 (5): 677–683. doi:10.1002/art.1780240508. ISSN 0004-3591.
- Moulton SJ, Kransdorf MJ, Ginsburg WW, Abril A, Persellin S (March 2005). "Eosinophilic fasciitis: spectrum of MRI findings". AJR. American journal of roentgenology. 184 (3): 975–8. doi:10.2214/ajr.184.3.01840975. PMID 15728627. Retrieved 2012-08-30.