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Half-and-half nail
Anirban Das, Sabyasachi Choudhury, Sudipta Pandit, Sibes K
Das
A 37-year-old man with uncontrolled hypertension for last 7
years presented with progressive shortness of breath for 2 months. Laboratory
evaluation revealed haemoglobin 7.2 g/dL, fasting plasma glucose 96 mg/dL, blood
urea nitrogen 122 mg/dL, serum creatinine 7.3 mg/dL, sodium 125 mEq/L, and
potassium 6.3 mEq/L.
On examination, his fingernails had a pink transverse band
distally and dull whitening of the proximal nail beds (Figure 1).
Figure 1. Fingernails showing half-and-half
nail changes
![]() Half-and-half nails (brown arcs or Lindsay’s nail)
show red, pink or brown distal bands occupying 20–60% of total nail length
with the remaining proximal portion exhibiting a dull white ground glass
appearance. The line of demarcation is sharp and runs parallel to the distal or
free margin of the nail.
It was first reported by Bean in
1963.1 It is more common in fingernails but may
occur in toenails. This disorder is commonly found in patients with chronic
kidney disease and infrequently with Behcet’s syndrome, yellow nail
syndrome with hyperthyroidism, pellegra, and in healthy persons.
Frequency of half-and-half nail changes in renal failure
varies between 20–50% and there is no correlation between severity of
renal disease and the length of the distal bands. The lesion often appears early
and remains permanent even after haemodialysis, but disappears completely within
2 to 3 weeks after successful renal transplant.
It was proposed that the discoloration was secondary to
melanin deposition in the distal portion of the nail
plate.2 Possibly the toxic substances of
uraemia stimulate the nail matrix melanocytes to produce melanin, and the
associated slow nail growth in renal failure results in large accumulation of
the pigment. Others postulated that increase in the number of capillaries and
thickening of the capillary walls in the nail beds were responsible for the
lesion.3
The presence of these nail changes warrants thorough
evaluation to exclude chronic kidney disease.
Author information: Anirban Das, Assistant
Professor; Sabyasachi Choudhury, RMO cum Clinical Tutor; Sudipta Pandit,
Associate Professor; Sibes K Das, Professor; Department of Pulmonary Medicine,
Medical College, Kolkata, West Bengal, India
Correspondence: Anirban Das, Department of
Pulmonary Medicine, Medical College, Kolkata, West Bengal, India, 700 073.
Email: dranirbandas_chest@rediffmail.com
References:
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