TY - JOUR UR - https://doi.org/10.25259/IJDVL_1203_20 DO - 10.25259/IJDVL_1203_20 TI - Clinical and radiological assessment of rhinomaxillary syndrome in Hansen’s disease AU - do Espírito Santo,Rachel Bertolani AU - Serafim,Rachel Azevedo AU - Loureiro,Rafael Maffei AU - Sumi,Daniel Vaccaro AU - de Mello,Ricardo Andrade Fernandes AU - Nascimento,Izabelle Felix AU - Lee,Arthur Ferraz Jong Mun AU - Collin,John D. AU - Collin,Simon M. AU - Deps,Patrícia AB - Background More than four million people today live with Hansen’s disease, and 200,000 new cases are diagnosed every year. Lifetime effects of Hansen’s disease manifest as changes to bones of the face, hands and feet, resulting in physical impairment, secondary complications and facial changes that can be detrimental to quality of life, particularly among the elderly. Aims This study aimed to perform a detailed characterization of rhinomaxillary syndrome and its clinical manifestations in older persons treated in the past for Hansen’s disease. Methods This was a cross-sectional study to characterize rhinomaxillary syndrome among older persons (age 60+ years) resident at Pedro Fontes Hospital, Cariacica, Espírito Santo, Brazil. Computed tomography images were examined with three-dimensional reconstructions to assess alterations to maxillofacial bones according to criteria for radiological rhinomaxillary syndrome. Participants were examined to assess facial alterations according to criteria for clinical rhinomaxillary syndrome. Results Rhinomaxillary syndrome was investigated in 16 participants (ten females and six males), median age 70 (range 60–89) years, age at diagnosis 20 (6–43) years and time since diagnosis 46 (26–70) years. Four participants fully met radiological rhinomaxillary syndrome criteria, four partially. All participants with full radiological rhinomaxillary syndrome presented with facial changes which met criteria for clinical rhinomaxillary syndrome, including “saddle nose” (loss of nasal dorsal height and shortened length of nose, due to cartilaginous and/or bone collapse), concave middle third of the face with sunken nose, maxillary retrognathia and inverted upper lip. Limitations Clinical histories were incomplete for some participants because records were lost at the hospital over time. Conclusion Until Hansen’s disease is eliminated from endemic countries, persons affected will continue to present with rhinomaxillofacial alterations caused by Mycobacterium leprae infection. Clinical protocols for assessment and long-term care need to include otorhinolaryngological evaluation, mainly to prevent secondary complications. When rhinomaxillofacial bone changes are suspected, this evaluation should be supported by computed tomography imaging, if available. VL - 88 T2 - Indian Journal of Dermatology, Venereology and Leprology JO - Indian Journal of Dermatology, Venereology and Leprology J2 - Indian Journal of Dermatology, Venereology and Leprology SN - 0378-6323 SN - 0973-3922 ER -