J Neuroanaesth Crit Care 2015; 02(02): 136-138
DOI: 10.4103/2348-0548.154242
Case Report
Thieme Medical and Scientific Publishers Private Ltd.

Maffucci syndrome: Anaesthetic management and review of literature

Gyaninder P Singh
1   Department of Neuroanaesthesiology, All India Institute of Medical Sciences, New Delhi, India
,
Barkha Bindu
1   Department of Neuroanaesthesiology, All India Institute of Medical Sciences, New Delhi, India
,
Mihir P Pandia
1   Department of Neuroanaesthesiology, All India Institute of Medical Sciences, New Delhi, India
,
Parmod K Bithal
1   Department of Neuroanaesthesiology, All India Institute of Medical Sciences, New Delhi, India
› Author Affiliations

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Publication History

Publication Date:
02 May 2018 (online)

Abstract

Maffucci syndrome is a rare, nonhereditary disorder manifesting early in life. The syndrome is characterized by presence of multiple hemangiomas and enchondromas mostly affecting the extremities. Haemangiomas are usually cutaneous, but may sometimes be visceral as well. Enchondromas commonly affect the long bones of the extremities. However, other areas including skull, ribs, vertebrae, larynx and trachea may also be involved. The presence of these lesions in the trachea and/or oropharynx may compromise the airway and cause difficulty during tracheal intubation. Complete airway examination and investigation is important to rule out any such lesion in a patient of Maffucci syndrome before planning for general anaesthesia with tracheal intubation.