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Analysis of symmetricity in the three different (sagittal, transverse and frontal) planes in generalized nonsegmental vitiligo. | LitMetric

AI Article Synopsis

  • Nonsegmental vitiligo is often thought to be symmetrical, but this study investigates how valid that idea is by examining clinical characteristics and lesion patterns in patients.
  • A study of 712 patients revealed that 78% showed bilateral involvement, with some areas of the body having more similarity in lesion distribution than others.
  • The findings suggest that there's significant symmetry in vitiligo lesions, which could help in creating a better understanding of the disease and potentially improve patient care.

Article Abstract

Background: Nonsegmental vitiligo is defined as being "often symmetrical", however, no work has tackled the point as to how valid it is to depend upon the concept of symmetricity in generalized nonsegmental vitiligo.

Aims: To investigate vitiligo symmetry, taking into account sites of predilection, the clinical characteristics of patients were studied.

Methods: This multicentric study included 712 nonsegmental vitiligo patients with 2876 examined lesions. Three models were drawn for each patient. Sagittal, transverse and frontal planes were drawn to divide the body into right/left, upper/lower and anterior/posterior halves respectively. Patients were examined by Wood's light and analyzed for symmetry.

Results: Bilateral involvement was present in 78% (P < 0.001). Studying the similarity of clinical involvement in the upper and lower body parts revealed that such similarity was present in 38%, with a significant positive association in some areas. Studying clinical similarity in the anteroposterior distribution pattern revealed a significant positive association in 11%.

Limitations: Relatively low number of patients.

Conclusions: We found significant bilateral symmetry in the lesions of 78% of vitiligo patients. Our work could aid in drawing the anticipated vitiligo map in patients with active disease, helping in increasing our understanding of the clinical behaviour of this disease.

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Source
http://dx.doi.org/10.4103/ijdvl.IJDVL_979_19DOI Listing

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