Schilder's disease: Difference between revisions
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:This article deals with the MS variant known as '''diffuse myelinoclastic sclerosis'''. For the leukodystrophy described by | :This article deals with the MS variant known as '''diffuse myelinoclastic sclerosis'''. For the leukodystrophy described by Paul Schilder and [[Thomas Addison]], sometimes known as Schilder's disease, see [[Adrenoleukodystrophy]] | ||
{{Infobox_Disease | | {{Infobox_Disease | | ||
Name = {{PAGENAME}} | | Name = {{PAGENAME}} | | ||
Revision as of 03:15, 16 January 2009
- This article deals with the MS variant known as diffuse myelinoclastic sclerosis. For the leukodystrophy described by Paul Schilder and Thomas Addison, sometimes known as Schilder's disease, see Adrenoleukodystrophy
| Schilder's disease | |
| ICD-9 | 341.1 |
|---|---|
| OMIM | 272100 |
| DiseasesDB | 11849 |
| eMedicine | neuro/92 |
| MeSH | D002549 |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]
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Overview
Schilder's disease or diffuse myelinoclastic sclerosis is a a very infrequent neurodegenerative disease that presents clinically as pseudotumoural demyelinating lesions, that make its diagnosis difficult. It presents adrenal atrophy and diffuse cerebral demyelination. It usually begins in childhood, affecting children between 5 and 14 years old.[1][2]
This disease is considered one of the borderline forms of multiple sclerosis because some authors consider them different diseases and others MS variants. Other diseases in this group are neuromyelitis optica (NMO), Balo concentric sclerosis and Marburg multiple sclerosis[3].
Symptoms
Symptoms are similar to those in multiple sclerosis and may include dementia, aphasia, seizures, personality changes, poor attention, tremors, balance instability, incontinence, muscle weakness, headache, vomiting, and vision and speech impairment.[4]
Diagnostic
The Poser criteria for diagnosis are:[5]
- One or two roughly symmetrical large plaques. Plaques are greater than 2 cm diameter.
- No other lesions are present and there are no abnormalities of the peripheral nervous system.
- Results of adrenal function studies and serum very long chain fatty acids are normal.
- Pathological analysis is consistent with subacute or chronic myelinoclastic diffuse sclerosis.
Prognosis and clinical course
The prognosis of this disease is very variable and can take three different courses: a monofasic, not remitting; [6] [7], remitting;[8] [9] [10] and finally, progressive, with increase in deficits.[11]
Treatments
Management Corticosteroids may be effective in some patients. Otherwise management in supportive and includes physiotherapy, occupational therapy and nutritional support in the later stages
History
It was first described by Paul Ferdinand Schilder in 1912,[12][13] and for a hundred years the term was used to describe also the other white matter pathologies described by him[14]. In 1986 Poser restricted its use to the disease described here.
References
- ↑ Garrido C, Levy-Gomes A, Teixeira J, Temudo T (2004). "[Schilder's disease: two new cases and a review of the literature]". Revista de neurologia (in Spanish). 39 (8): 734–8. PMID 15514902.
- ↑ Afifi AK, Bell WE, Menezes AH, Moore SA (1994). "Myelinoclastic diffuse sclerosis (Schilder's disease): report of a case and review of the literature". J. Child Neurol. 9 (4): 398–403. PMID 7822732.
- ↑ Fontaine B (2001). "[Borderline forms of multiple sclerosis]". Rev. Neurol. (Paris) (in French). 157 (8-9 Pt 2): 929–34. PMID 11787357.
- ↑ NINDS Schilder's Disease Information Page [1]
- ↑ Poser CM, Goutières F, Carpentier MA, Aicardi J (1986). "Schilder's myelinoclastic diffuse sclerosis". Pediatrics. 77 (1): 107–12. PMID 3940347.
- ↑ Afifi AK, Bell WE, Menezes AH, Moore SA (1994). "Myelinoclastic diffuse sclerosis (Schilder's disease): report of a case and review of the literature". J. Child Neurol. 9 (4): 398–403. PMID 7822732.
- ↑ Pretorius ML, Loock DB, Ravenscroft A, Schoeman JF (1998). "Demyelinating disease of Schilder type in three young South African children: dramatic response to corticosteroids". J. Child Neurol. 13 (5): 197–201. PMID 9620009.
- ↑ de Lacour A, Guisado F, Zambrano A, Argente J, Acosta J, Ramos C (1998). "[Pseudotumor forms of demyelinating diseases. Report of three cases and review of the literature]". Revista de neurologia (in Spanish; Castilian). 27 (160): 966–70. PMID 9951014.
- ↑ Leuzzi V, Lyon G, Cilio MR, Pedespan JM, Fontan D, Chateil JF, Vital A (1999). "Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases". J. Neurol. Neurosurg. Psychiatr. 66 (3): 407–8. PMID 10084548.
- ↑ Brunot E, Marcus JC (1999). "Multiple sclerosis presenting as a single mass lesion". Pediatr. Neurol. 20 (5): 383–6. PMID 10371386.
- ↑ Garell PC, Menezes AH, Baumbach G, Moore SA, Nelson G, Mathews K, Afifi AK (1998). "Presentation, management and follow-up of Schilder's disease". Pediatric neurosurgery. 29 (2): 86–91. PMID 9792962.
- ↑ Template:WhoNamedIt
- ↑ P. F. Schilder, Zur Kenntnis der sogenannten diffusen Sklerose (über Encephalitis periaxialis diffusa). Zeitschrift für die gesamte Neurologie und Psychiatrie, 1912, 10 Orig.: 1-60.
- ↑ Martin JJ, Guazzi GC (1991). "Schilder's diffuse sclerosis". Dev. Neurosci. 13 (4–5): 267–73. PMID 1817032.
See also
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Multiple sclerosis Microchapters |
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Diagnosis |
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Treatment |
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Case Studies |
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Schilder's disease On the Web |
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American Roentgen Ray Society Images of Schilder's disease |