POEMS syndrome historical perspective: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
|||
| (2 intermediate revisions by the same user not shown) | |||
| Line 3: | Line 3: | ||
{{CMG}}{{AE}}{{Sab}} | {{CMG}}{{AE}}{{Sab}} | ||
==Overview== | ==Overview== | ||
In 1938, Ilya Mark Scheinker, a Russian neurologist and neuropathologist described a patient with a solitary plasmacytoma, sensorimotor polyneuropathy, and localized patches of thickened and deeply pigmented skin. In 1956, R. S. Crow published two case reports of myelomatosis with peripheral neuritis and other striking features. In 1977, Iwashita et al described a patient who had an osteosclerotic myeloma accompanied by sensorimotor polyneuropathy, skin hyperipigmentation, edema, hypertrichosis, gynecomastia, and white nails. In 1980, Bardwick et al proposed the acronym 'POEMS' to represent a syndrome characterized by polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes. | In 1938, Ilya Mark Scheinker, a Russian [[Neurology|neurologist]] and [[Neuropathology|neuropathologist]] described a [[patient]] with a solitary plasmacytoma, [[sensorimotor]] [[polyneuropathy]], and localized patches of thickened and deeply [[Pigment|pigmented]] [[skin]]. In 1956, R. S. Crow published two case reports of myelomatosis with [[Neuritis|peripheral neuritis]] and other striking features. In 1977, Iwashita et al described a [[patient]] who had an [[Osteosclerosis|osteosclerotic]] [[Multiple myeloma|myeloma]] accompanied by [[sensorimotor]] [[polyneuropathy]], [[skin]] [[Pigment|hyperipigmentation]], [[edema]], [[hypertrichosis]], [[gynecomastia]], and white [[Nail (anatomy)|nails]]. In 1980, Bardwick et al proposed the acronym 'POEMS' to represent a [[syndrome]] characterized by [[polyneuropathy]], [[organomegaly]], [[Endocrinology|endocrinopathy]], [[M protein]], and [[skin]] changes. | ||
==Historical Perspective== | ==Historical Perspective== | ||
===Discovery=== | ===Discovery=== | ||
*In 1938, Ilya Mark Scheinker, a Russian neurologist and neuropathologist described a patient with a solitary plasmacytoma, sensorimotor polyneuropathy, and localized patches of thickened and deeply pigmented skin.<ref name="Dispenzieri2002">{{cite journal|last1=Dispenzieri|first1=A.|title=POEMS syndrome: definitions and long-term outcome|journal=Blood|volume=101|issue=7|year=2002|pages=2496–2506|issn=00064971|doi=10.1182/blood-2002-07-2299}}</ref><ref>Scheinker I. Myelom und Nervensystem: über eine bisher nicht beschriebene mit eigentümlichen Hautveränderungen einhergehende Polyneuritis bei einem plasmazellulären myelom des Sternums. Dtsch Z Nervenheilkd 1938; 147: 247</ref> | *In 1938, Ilya Mark Scheinker, a Russian [[Neurology|neurologist]] and [[Neuropathology|neuropathologist]] described a [[patient]] with a solitary plasmacytoma, [[sensorimotor]] [[polyneuropathy]], and localized patches of thickened and deeply [[Pigment|pigmented]] [[skin]].<ref name="Dispenzieri2002">{{cite journal|last1=Dispenzieri|first1=A.|title=POEMS syndrome: definitions and long-term outcome|journal=Blood|volume=101|issue=7|year=2002|pages=2496–2506|issn=00064971|doi=10.1182/blood-2002-07-2299}}</ref><ref>Scheinker I. Myelom und Nervensystem: über eine bisher nicht beschriebene mit eigentümlichen Hautveränderungen einhergehende Polyneuritis bei einem plasmazellulären myelom des Sternums. Dtsch Z Nervenheilkd 1938; 147: 247</ref> | ||
*POEMS syndrome has been recognized by various names over the years, such as osteosclerotic myeloma, Crow-Fukase syndrome, PEP syndrome, and Takatsuki syndrome.<ref name="Dispenzieri2002">{{cite journal|last1=Dispenzieri|first1=A.|title=POEMS syndrome: definitions and long-term outcome|journal=Blood|volume=101|issue=7|year=2002|pages=2496–2506|issn=00064971|doi=10.1182/blood-2002-07-2299}}</ref> | *POEMS [[syndrome]] has been recognized by various names over the years, such as [[Osteosclerosis|osteosclerotic]] [[Multiple myeloma|myeloma]], Crow-Fukase [[syndrome]], [[PEP|PEP syndrome]], and Takatsuki [[syndrome]].<ref name="Dispenzieri2002">{{cite journal|last1=Dispenzieri|first1=A.|title=POEMS syndrome: definitions and long-term outcome|journal=Blood|volume=101|issue=7|year=2002|pages=2496–2506|issn=00064971|doi=10.1182/blood-2002-07-2299}}</ref> | ||
*In 1956, R. S. Crow published two case reports of myelomatosis with peripheral neuritis and other striking features.<ref name="pmid13364332">{{cite journal |vauthors=CROW RS |title=Peripheral neuritis in myelomatosis |journal=Br Med J |volume=2 |issue=4996 |pages=802–4 |date=October 1956 |pmid=13364332 |pmc=2035359 |doi= |url=}}</ref> | *In 1956, R. S. Crow published two case reports of myelomatosis with [[Neuritis|peripheral neuritis]] and other striking features.<ref name="pmid13364332">{{cite journal |vauthors=CROW RS |title=Peripheral neuritis in myelomatosis |journal=Br Med J |volume=2 |issue=4996 |pages=802–4 |date=October 1956 |pmid=13364332 |pmc=2035359 |doi= |url=}}</ref> | ||
*In 1977, Iwashita et al described a patient who had an osteosclerotic myeloma accompanied by sensorimotor polyneuropathy, skin hyperipigmentation, edema, hypertrichosis, gynecomastia, and white nails.<ref name="pmid559975">{{cite journal |vauthors=Iwashita H, Ohnishi A, Asada M, Kanazawa Y, Kuroiwa Y |title=Polyneuropathy, skin hyperpigmentation, edema, and hypertrichosis in localized osteosclerotic myeloma |journal=Neurology |volume=27 |issue=7 |pages=675–81 |date=July 1977 |pmid=559975 |doi= |url=}}</ref> | *In 1977, Iwashita et al described a [[patient]] who had an [[Osteosclerosis|osteosclerotic]] [[Multiple myeloma|myeloma]] accompanied by [[sensorimotor]] [[polyneuropathy]], [[skin]] [[Pigment|hyperipigmentation]], edema, [[hypertrichosis]], [[gynecomastia]], and white [[Nail (anatomy)|nails]].<ref name="pmid559975">{{cite journal |vauthors=Iwashita H, Ohnishi A, Asada M, Kanazawa Y, Kuroiwa Y |title=Polyneuropathy, skin hyperpigmentation, edema, and hypertrichosis in localized osteosclerotic myeloma |journal=Neurology |volume=27 |issue=7 |pages=675–81 |date=July 1977 |pmid=559975 |doi= |url=}}</ref> | ||
*In 1980, Bardwick et al proposed the acronym 'POEMS' to represent a syndrome characterized by polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes.<ref name="pmid6248720">{{cite journal |vauthors=Bardwick PA, Zvaifler NJ, Gill GN, Newman D, Greenway GD, Resnick DL |title=Plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes: the POEMS syndrome. Report on two cases and a review of the literature |journal=Medicine (Baltimore) |volume=59 |issue=4 |pages=311–22 |date=July 1980 |pmid=6248720 |doi= |url=}}</ref> | *In 1980, Bardwick et al proposed the acronym 'POEMS' to represent a [[syndrome]] characterized by [[polyneuropathy]], [[organomegaly]], [[Endocrinology|endocrinopathy]], [[M protein]], and [[skin]] changes.<ref name="pmid6248720">{{cite journal |vauthors=Bardwick PA, Zvaifler NJ, Gill GN, Newman D, Greenway GD, Resnick DL |title=Plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes: the POEMS syndrome. Report on two cases and a review of the literature |journal=Medicine (Baltimore) |volume=59 |issue=4 |pages=311–22 |date=July 1980 |pmid=6248720 |doi= |url=}}</ref> | ||
===Synonyms of POEMS syndrome=== | |||
*Crow-Fukase [[syndrome]]<ref>https://rarediseases.org/rare-diseases/poems-syndrome/</ref> | |||
*[[Osteosclerosis|Osteosclerotic]] [[Multiple myeloma|myeloma]]<ref>https://rarediseases.org/rare-diseases/poems-syndrome/</ref> | |||
*[[PEP|PEP syndrome]]<ref>https://rarediseases.org/rare-diseases/poems-syndrome/</ref> | |||
*[[Polyneuropathy]]-[[organomegaly]]-[[Endocrinology|endocrinopathy]]-[[M protein]]-[[Skin lesion|skin lesions]]<ref>https://rarediseases.org/rare-diseases/poems-syndrome/</ref> | |||
*Shimpo [[syndrome]]<ref>https://rarediseases.org/rare-diseases/poems-syndrome/</ref> | |||
*Takatsuki [[syndrome]]<ref>https://rarediseases.org/rare-diseases/poems-syndrome/</ref> | |||
==References== | ==References== | ||
Latest revision as of 02:11, 4 February 2019
|
POEMS syndrome Microchapters |
|
Diagnosis |
|---|
|
Treatment |
|
Case Studies |
|
POEMS syndrome historical perspective On the Web |
|
American Roentgen Ray Society Images of POEMS syndrome historical perspective |
|
Risk calculators and risk factors for POEMS syndrome historical perspective |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Sabawoon Mirwais, M.B.B.S, M.D.[2]
Overview
In 1938, Ilya Mark Scheinker, a Russian neurologist and neuropathologist described a patient with a solitary plasmacytoma, sensorimotor polyneuropathy, and localized patches of thickened and deeply pigmented skin. In 1956, R. S. Crow published two case reports of myelomatosis with peripheral neuritis and other striking features. In 1977, Iwashita et al described a patient who had an osteosclerotic myeloma accompanied by sensorimotor polyneuropathy, skin hyperipigmentation, edema, hypertrichosis, gynecomastia, and white nails. In 1980, Bardwick et al proposed the acronym 'POEMS' to represent a syndrome characterized by polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes.
Historical Perspective
Discovery
- In 1938, Ilya Mark Scheinker, a Russian neurologist and neuropathologist described a patient with a solitary plasmacytoma, sensorimotor polyneuropathy, and localized patches of thickened and deeply pigmented skin.[1][2]
- POEMS syndrome has been recognized by various names over the years, such as osteosclerotic myeloma, Crow-Fukase syndrome, PEP syndrome, and Takatsuki syndrome.[1]
- In 1956, R. S. Crow published two case reports of myelomatosis with peripheral neuritis and other striking features.[3]
- In 1977, Iwashita et al described a patient who had an osteosclerotic myeloma accompanied by sensorimotor polyneuropathy, skin hyperipigmentation, edema, hypertrichosis, gynecomastia, and white nails.[4]
- In 1980, Bardwick et al proposed the acronym 'POEMS' to represent a syndrome characterized by polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes.[5]
Synonyms of POEMS syndrome
- Crow-Fukase syndrome[6]
- Osteosclerotic myeloma[7]
- PEP syndrome[8]
- Polyneuropathy-organomegaly-endocrinopathy-M protein-skin lesions[9]
- Shimpo syndrome[10]
- Takatsuki syndrome[11]
References
- ↑ 1.0 1.1 Dispenzieri, A. (2002). "POEMS syndrome: definitions and long-term outcome". Blood. 101 (7): 2496–2506. doi:10.1182/blood-2002-07-2299. ISSN 0006-4971.
- ↑ Scheinker I. Myelom und Nervensystem: über eine bisher nicht beschriebene mit eigentümlichen Hautveränderungen einhergehende Polyneuritis bei einem plasmazellulären myelom des Sternums. Dtsch Z Nervenheilkd 1938; 147: 247
- ↑ CROW RS (October 1956). "Peripheral neuritis in myelomatosis". Br Med J. 2 (4996): 802–4. PMC 2035359. PMID 13364332.
- ↑ Iwashita H, Ohnishi A, Asada M, Kanazawa Y, Kuroiwa Y (July 1977). "Polyneuropathy, skin hyperpigmentation, edema, and hypertrichosis in localized osteosclerotic myeloma". Neurology. 27 (7): 675–81. PMID 559975.
- ↑ Bardwick PA, Zvaifler NJ, Gill GN, Newman D, Greenway GD, Resnick DL (July 1980). "Plasma cell dyscrasia with polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes: the POEMS syndrome. Report on two cases and a review of the literature". Medicine (Baltimore). 59 (4): 311–22. PMID 6248720.
- ↑ https://rarediseases.org/rare-diseases/poems-syndrome/
- ↑ https://rarediseases.org/rare-diseases/poems-syndrome/
- ↑ https://rarediseases.org/rare-diseases/poems-syndrome/
- ↑ https://rarediseases.org/rare-diseases/poems-syndrome/
- ↑ https://rarediseases.org/rare-diseases/poems-syndrome/
- ↑ https://rarediseases.org/rare-diseases/poems-syndrome/