Korean J Clin Neurophysiol.  2013 Jun;15(1):19-23. 10.14253/kjcn.2013.15.1.19.

Leprous Neuropathy Associated with Predominant Proprioceptive Sensory Loss

Affiliations
  • 1Pusan National University School of Medicine, Busan, Korea. dskim@pusan.ac.kr
  • 2Department of Neurology, Pusan National University Yangsan Hospital, Busan, Korea.
  • 3Reseach Institute for Convergence of Biomedical Science and Technology, Pusan National University Yangsan Hospital, Busan, Korea.

Abstract

Some patients with leprosy may present with atypical features, such as isolated peripheral neuropathy without skin lesions, or marked proprioceptive dysfunction. We report a 56-year-old female who presented with predominant proprioceptive loss without skin lesion, but was finally confirmed as leprous neuropathy by sural nerve biopsy. It is postulated that large myelinated fibers were affected by chronic immunological reactions triggered by inactive bacterial particles, producing a peripheral neuropathy presenting as predominant proprioceptive sensory loss without typical skin lesions.

Keyword

Leprosy; Proprioception; Peripheral neuropathy

MeSH Terms

Biopsy
Female
Humans
Leprosy
Myelin Sheath
Organic Chemicals
Peripheral Nervous System Diseases
Proprioception
Skin
Sural Nerve
Organic Chemicals

Figure

  • Figure 1. Sural nerve biopsy findings of the patient. (A) Almost complete loss of myelinated nerve fibers was observed with thickening and hypertrophy of epineurial sheath (H&E stain ×100). (B) On longitudinal sections, perivascular inflammatory infiltrates were prominent (Modified Gomori-trichrome stain ×100). (C) A non-caseating granuloma with giant cells are seen (H&E stain ×400). (D) On Fite stain, no acid-fast bacilli were observed (Fite stain, ×100). The black bars represent 100 μm.


Reference

1.Ooi WW., Srinivasan J. Leprosy and the peripheral nervous system: basic and clinical aspects. Muscle Nerve. 2004. 30:393–409.
Article
2.WHO. Global leprosy situation, 2010. Wkly Epidemiol Rec. 2010. 85:337.
3.Agrawal A., Pandit L., Dalal M., Shetty JP. Neurological manifestations of Hansen’s disease and their management. Clin Neurol Neurosurg. 2005. 107:445–454.
Article
4.Skacel M., Antunes SL., Rodrigues MM., Nery JA., Valentim VD., Morais RP, et al. The diagnosis of leprosy among patients with symptoms of peripheral neuropathy without cutaneous lesions: a follow-up study. Arq Neuropsiquiatr. 2000. 58:800–807.
Article
5.Pandya SS., Bhakti WS. Severe pan-sensory neuropathy in leprosy. Int J Lepr Other Mycobact Dis. 1994. 62:24–31.
6.van Brakel WH., Nicholls PG., Das L., Barkataki P., Suneetha SK., Jadhav RS, et al. The INFIR Cohort Study: Investigating prediction, detection and pathogenesis of neuropathy and reactions in leprosy, Methods and baseline results of a cohort of multibacillary leprosy patients in north India. Lepr Rev. 2005. 76:14–34.
Article
7.Khadilkar SV., Benny R., Kasegaonkar PS. Proprioceptive loss in leprous neuropathy: a study of 19 patients. Neurol India. 2008. 56:450–455.
Article
8.Rosenberg NR., Faber WR., Vermeulen M. Unexplained delayed nerve impairment in leprosy after treatment. Lepr Rev. 2003. 74:357–365.
Article
9.Ha YM. Relapse of Leprosy. Korean Lepr Bull. 1994. 27:27–29.
10.THELEP: Persisting Mycobacterium leprae among THELEP trial patients in Bamako and Chingleput. Subcommittee on Clinical Trials of the Chemotherapy of Leprosy (THELEP) Scientific Working Group of the UNDP/World Bank/WHO Special Programme for Research and Training in Tropical Diseases. Lepr Rev. 1987. 58:325–337.
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