Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease)

Dercum’s disease (Dercum’s syndrome, neurolipomatosis) is a rare and inadequately studied chronic disease that is characterized by subcutaneous fatty deposits in different parts of the trunk and accompanied by compression-ischemic neuropathy of the cutaneous branches of peripheral nerves with pain s...
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Autor*in:	N. A. Shnayder [verfasserIn] I. A. Kiselev [verfasserIn] D. V. Dmitrenko [verfasserIn]

Format:	E-Artikel
Sprache:	Russisch

Erschienen:	2015

Schlagwörter:	синдром деркума нейролипоматоз болезненный липоматоз гендерные аспекты патогенез клиника диагностика дифференциальная диагностика лечение прогноз клинический случай

Übergeordnetes Werk:	In: Нервно-мышечные болезни - ABV-press, 2016, (2015), 2, Seite 45-52
Übergeordnetes Werk:	year:2015 ; number:2 ; pages:45-52

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc Journal toc

DOI / URN:	10.17650/2222-8721-2013-0-2-

Katalog-ID:	DOAJ000327484

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520			\|a Dercum’s disease (Dercum’s syndrome, neurolipomatosis) is a rare and inadequately studied chronic disease that is characterized by subcutaneous fatty deposits in different parts of the trunk and accompanied by compression-ischemic neuropathy of the cutaneous branches of peripheral nerves with pain syndrome, pathological fatigue, and obesity. The most common site of subcutaneous deposits is the upper extremities, elbows, anterior abdominal wall, buttocks, thighs, and knees. However, Dercum’s disease is systemic and can be manifested by a wide range of symptoms and it frequently recurs, including after surgical removal of lipomas. The paper presents a case of the late diagnosis of neurolipomatosis in a 23-year-old male. It considers the etiology, pathogenesis, and diagnosis of the disease and current approaches to its treatment. A better understanding of the characteristic clinical syndrome of painful lipomatosis will assist in the early diagnosis of the disease and in the prevention of inadequate therapy cases.
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653		0	\|a Neurology. Diseases of the nervous system
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allfieldsGer	10.17650/2222-8721-2013-0-2- doi (DE-627)DOAJ000327484 (DE-599)DOAJ59eb1b1bb44d49eda7e8a352c492ddd7 DE-627 ger DE-627 rakwb rus RC346-429 N. A. Shnayder verfasserin aut Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease) 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Dercum’s disease (Dercum’s syndrome, neurolipomatosis) is a rare and inadequately studied chronic disease that is characterized by subcutaneous fatty deposits in different parts of the trunk and accompanied by compression-ischemic neuropathy of the cutaneous branches of peripheral nerves with pain syndrome, pathological fatigue, and obesity. The most common site of subcutaneous deposits is the upper extremities, elbows, anterior abdominal wall, buttocks, thighs, and knees. However, Dercum’s disease is systemic and can be manifested by a wide range of symptoms and it frequently recurs, including after surgical removal of lipomas. The paper presents a case of the late diagnosis of neurolipomatosis in a 23-year-old male. It considers the etiology, pathogenesis, and diagnosis of the disease and current approaches to its treatment. A better understanding of the characteristic clinical syndrome of painful lipomatosis will assist in the early diagnosis of the disease and in the prevention of inadequate therapy cases. синдром деркума нейролипоматоз болезненный липоматоз гендерные аспекты патогенез клиника диагностика дифференциальная диагностика лечение прогноз клинический случай Neurology. Diseases of the nervous system I. A. Kiselev verfasserin aut D. V. Dmitrenko verfasserin aut In Нервно-мышечные болезни ABV-press, 2016 (2015), 2, Seite 45-52 (DE-627)1736677187 24130443 nnns year:2015 number:2 pages:45-52 https://doi.org/10.17650/2222-8721-2013-0-2- kostenfrei https://doaj.org/article/59eb1b1bb44d49eda7e8a352c492ddd7 kostenfrei https://nmb.abvpress.ru/jour/article/view/49 kostenfrei https://doaj.org/toc/2222-8721 Journal toc kostenfrei https://doaj.org/toc/2413-0443 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2015 2 45-52
allfieldsSound	10.17650/2222-8721-2013-0-2- doi (DE-627)DOAJ000327484 (DE-599)DOAJ59eb1b1bb44d49eda7e8a352c492ddd7 DE-627 ger DE-627 rakwb rus RC346-429 N. A. Shnayder verfasserin aut Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease) 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Dercum’s disease (Dercum’s syndrome, neurolipomatosis) is a rare and inadequately studied chronic disease that is characterized by subcutaneous fatty deposits in different parts of the trunk and accompanied by compression-ischemic neuropathy of the cutaneous branches of peripheral nerves with pain syndrome, pathological fatigue, and obesity. The most common site of subcutaneous deposits is the upper extremities, elbows, anterior abdominal wall, buttocks, thighs, and knees. However, Dercum’s disease is systemic and can be manifested by a wide range of symptoms and it frequently recurs, including after surgical removal of lipomas. The paper presents a case of the late diagnosis of neurolipomatosis in a 23-year-old male. It considers the etiology, pathogenesis, and diagnosis of the disease and current approaches to its treatment. A better understanding of the characteristic clinical syndrome of painful lipomatosis will assist in the early diagnosis of the disease and in the prevention of inadequate therapy cases. синдром деркума нейролипоматоз болезненный липоматоз гендерные аспекты патогенез клиника диагностика дифференциальная диагностика лечение прогноз клинический случай Neurology. Diseases of the nervous system I. A. Kiselev verfasserin aut D. V. Dmitrenko verfasserin aut In Нервно-мышечные болезни ABV-press, 2016 (2015), 2, Seite 45-52 (DE-627)1736677187 24130443 nnns year:2015 number:2 pages:45-52 https://doi.org/10.17650/2222-8721-2013-0-2- kostenfrei https://doaj.org/article/59eb1b1bb44d49eda7e8a352c492ddd7 kostenfrei https://nmb.abvpress.ru/jour/article/view/49 kostenfrei https://doaj.org/toc/2222-8721 Journal toc kostenfrei https://doaj.org/toc/2413-0443 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 2015 2 45-52
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author	N. A. Shnayder
spellingShingle	N. A. Shnayder misc RC346-429 misc синдром деркума misc нейролипоматоз misc болезненный липоматоз misc гендерные аспекты misc патогенез misc клиника misc диагностика misc дифференциальная диагностика misc лечение misc прогноз misc клинический случай misc Neurology. Diseases of the nervous system Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease)
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topic_title	RC346-429 Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease) синдром деркума нейролипоматоз болезненный липоматоз гендерные аспекты патогенез клиника диагностика дифференциальная диагностика лечение прогноз клинический случай
topic	misc RC346-429 misc синдром деркума misc нейролипоматоз misc болезненный липоматоз misc гендерные аспекты misc патогенез misc клиника misc диагностика misc дифференциальная диагностика misc лечение misc прогноз misc клинический случай misc Neurology. Diseases of the nervous system
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title	Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease)
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title_sort	clinical case of the late diagnosis of neurolipomatosis (dercum’s disease)
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title_auth	Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease)
abstract	Dercum’s disease (Dercum’s syndrome, neurolipomatosis) is a rare and inadequately studied chronic disease that is characterized by subcutaneous fatty deposits in different parts of the trunk and accompanied by compression-ischemic neuropathy of the cutaneous branches of peripheral nerves with pain syndrome, pathological fatigue, and obesity. The most common site of subcutaneous deposits is the upper extremities, elbows, anterior abdominal wall, buttocks, thighs, and knees. However, Dercum’s disease is systemic and can be manifested by a wide range of symptoms and it frequently recurs, including after surgical removal of lipomas. The paper presents a case of the late diagnosis of neurolipomatosis in a 23-year-old male. It considers the etiology, pathogenesis, and diagnosis of the disease and current approaches to its treatment. A better understanding of the characteristic clinical syndrome of painful lipomatosis will assist in the early diagnosis of the disease and in the prevention of inadequate therapy cases.
abstractGer	Dercum’s disease (Dercum’s syndrome, neurolipomatosis) is a rare and inadequately studied chronic disease that is characterized by subcutaneous fatty deposits in different parts of the trunk and accompanied by compression-ischemic neuropathy of the cutaneous branches of peripheral nerves with pain syndrome, pathological fatigue, and obesity. The most common site of subcutaneous deposits is the upper extremities, elbows, anterior abdominal wall, buttocks, thighs, and knees. However, Dercum’s disease is systemic and can be manifested by a wide range of symptoms and it frequently recurs, including after surgical removal of lipomas. The paper presents a case of the late diagnosis of neurolipomatosis in a 23-year-old male. It considers the etiology, pathogenesis, and diagnosis of the disease and current approaches to its treatment. A better understanding of the characteristic clinical syndrome of painful lipomatosis will assist in the early diagnosis of the disease and in the prevention of inadequate therapy cases.
abstract_unstemmed	Dercum’s disease (Dercum’s syndrome, neurolipomatosis) is a rare and inadequately studied chronic disease that is characterized by subcutaneous fatty deposits in different parts of the trunk and accompanied by compression-ischemic neuropathy of the cutaneous branches of peripheral nerves with pain syndrome, pathological fatigue, and obesity. The most common site of subcutaneous deposits is the upper extremities, elbows, anterior abdominal wall, buttocks, thighs, and knees. However, Dercum’s disease is systemic and can be manifested by a wide range of symptoms and it frequently recurs, including after surgical removal of lipomas. The paper presents a case of the late diagnosis of neurolipomatosis in a 23-year-old male. It considers the etiology, pathogenesis, and diagnosis of the disease and current approaches to its treatment. A better understanding of the characteristic clinical syndrome of painful lipomatosis will assist in the early diagnosis of the disease and in the prevention of inadequate therapy cases.
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title_short	Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease)
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Clinical case of the late diagnosis of neurolipomatosis (Dercum’s disease)

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