Leprotic neuropathy misdiagnosed as chronic inflammatory demyelinating polyneuropathy
Author(s) -
Se Hoon Kim,
Ha Young Shin,
Seung Min Kim,
Ki-Han Kwon,
Yang Ki Minn
Publication year - 2012
Publication title -
leprosy review
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 43
eISSN - 2162-8807
pISSN - 0305-7518
DOI - 10.47276/lr.83.1.93
Subject(s) - medicine , chronic inflammatory demyelinating polyneuropathy , polyneuropathy , dermatology , immunology , surgery , antibody
Leprosy is a disease characteristically involving the skin and peripheral nerves. Leprosy is diagnosed typically by observation of representative skin lesions and the presence of acid-fast bacilli (AFB) in a skin smear or a skin biopsy; deepnerve biopsies such as a sural nerve biopsy are not routine procedures. Therefore, very few reports of sural nerve biopsies that yield a pathologic finding of leprosy are available; moreover, electron microscopic studies are still rarer. A nerve conduction study (NCS) and sural nerve biopsy are the gold standards for the diagnosis of chronic inflammatory polyneuropathy (CIDP). NCS findings that indicate leprosy are known as mononeuropathy pattern or mononeuritis multiplex pattern and these findings distinguish leprosy from demyelinating polyneuropathies such as CIDP. In non-endemic areas such as Korea, leprosy is not the most likely diagnosis to account for subacute peripheral nerve lesions. We report a case of lepromatous leprosy neuropathy that was misdiagnosed as CIDP after a nerve conduction study and a sural nerve biopsy.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom