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Two brothers with nail cyanosis
Ellis Hon and Albert Li
Cyanosis of fingers and nails in infants and children
deserves investigation and treatment of the underlying causes. It may be due to
a trivial condition such as acrocyanosis of well neonates, which requires no
treatment other than reassurance of the parents. On the other hand, serious
cardiopulmonary conditions need to be
excluded.1 These conditions include cyanotic
heart disease and chronic pulmonary conditions such as cystic fibrosis and
empyema. These conditions are usually accompanied by the clubbing of fingers.
Cyanosis without clubbing can also occur in Raynaud’s
phenomenon.1 We report the case of two brothers
with an unusual cause of ‘cyanosis’ of fingernails and
toenails.
Case reportA sixteen-year-old boy with good
past health was evaluated because his fingernails, and subsequently toenails,
had become blue over a four-week period. He was a nonsmoker and denied any
systemic symptoms, change of dietary habit, injury to the nails, or
medication/nail polish consumption. He wore white socks and his shoes were not
blue. Over the same period, his elder brother had also developed a similar blue
hue in his fingernails and toenails.
Figure 1. Appearance of the fingernails and toenails of
the patient who presents with nail ‘cyanosis’
![]() Physical examination revealed an apparently well teenager
with uniform cyanosis of his toenails, and to a lesser extent in his fingernails
(Figure 1). The pulps of his fingers and toes remained pink and the peripheral
arterial pulses were normal. Blanching of the finger and toe tips did not alter
the cyanosis, suggesting that the discolouration was in the nail plate rather
than the vascular nail bed. There was no central cyanosis or cardiopulmonary
abnormality and his examination was unremarkable. His oxygen saturation was 99%
in room air. Laboratory investigations were as follows: haemoglobin 14.0 g/dl;
white blood count 7.4x109/l with normal
differentials; platelet count 282x109/l.
Complement C3 was 1.31 g/l (reference range 0.62 to 1.87), and C4 was 0.27 g/l
(reference range 0.20 to 0.59). Liver function and renal function tests were
normal. Rheumatoid factor and anti-nuclear antibodies were negative. Urine
analysis was also unremarkable.
As there was no clubbing or cardiopulmonary abnormality to
explain his nail cyanosis, a nail-trim biopsy was scheduled in order to rule out
abnormal pigment deposition in the nail matrix. The ‘cyanosis’ was
accidentally removed by alcohol swab prior to nail biopsy. Further inquiry
revealed that the discolouration was due to the dye from new blankets purchased
and used by the two brothers in the preceding four weeks. Interestingly, the two
brothers used separate blankets and slept in separate rooms.
DiscussionNail discolouration due to dyeing
has not been reported as a differential diagnosis for peripheral cyanosis. In
our patient, there was no history of subungual haematoma or antimalarial use,
and no evidence of Raynaud’s phenomenon, central cyanosis or
cardiopulmonary disease. His oxygen saturation was good. The finger and nail
pulps remained pink and suggested that the problem primarily lay within the nail
parenchyma. Blue nails secondary to chronic silver exposure, alcaptonuria and
HIV have been reported in the
literature.2–4 Poisoning with a drug or
chemical should be suspected in any child who presents with sudden-onset
cyanosis. A number of compounds activate haemoglobin oxidation from the ferrous
to the ferric state to form methaemoglobin. These include nitrites and nitrate
(contaminated water), chlorates, quinines, aniline dyes, sulfonamides,
acetanilid, phenacetin bismuth subnitrate and potassium
chlorate.5–7 In a male with completely
negative clinical findings and normal oxygen saturations, we suggest that
‘dyed nails’ should be considered as a differential diagnosis of
nail cyanosis.
Author information:
Ellis KL Hon, Assistant Professor; Albert MC Li, Assistant Professor, Department
of Paediatrics, The Chinese University of Hong Kong, Prince of Wales Hospital,
Shatin, Hong Kong
Correspondence: Dr
Ellis KL Hon, Department of Paediatrics, The Chinese University of Hong Kong,
6/F, Clinical Sciences Building, Prince of Wales Hospital, Shatin, Hong Kong.
Fax: +852 2636 0020; email: ehon@hotmail.com
References:
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