|LETTER TO EDITOR
|Year : 2014 | Volume
| Issue : 3 | Page : 150-151
Congenital miliaria crystallina following maternal febrile illness
Thirunavukkarasu Arun Babu1, Vijayasankar Vijayadevagaran1, Vijayan Sharmila2
1 Department of Pediatrics, Indira Gandhi Medical College and Research Institute, Puducherry, India
2 Department of Obstetrics and Gynaecology, Indira Gandhi Medical College and Research Institute, Puducherry, India
|Date of Web Publication||30-Oct-2014|
Thirunavukkarasu Arun Babu
Associate Professor of Pediatrics, Indira Gandhi Medical College and Research, Institute, Puducherry
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Babu TA, Vijayadevagaran V, Sharmila V. Congenital miliaria crystallina following maternal febrile illness. Indian J Paediatr Dermatol 2014;15:150-1
|How to cite this URL:|
Babu TA, Vijayadevagaran V, Sharmila V. Congenital miliaria crystallina following maternal febrile illness. Indian J Paediatr Dermatol [serial online] 2014 [cited 2021 Jan 17];15:150-1. Available from: https://www.ijpd.in/text.asp?2014/15/3/150/143679
A term male, appropriate for gestational age baby was born to a 22-year-old G2A1 mother by spontaneous vaginal delivery. The baby was 3.4 kg, cried immediately after birth and had Apgar scores of 8 and 9 at 1 and 5 min, respectively. The neonate was found to have multiple, tiny, eruptions with clear fluid all over the body especially in the trunk and extremities.
Antenatal history revealed that mother was admitted with fever at 38 + 4 weeks, 1-week before the date of delivery. She was diagnosed to have lower respiratory infection and received oral antibiotics, antipyretics, and salbutamol nebulization for 3 days following which the fever subsided.
Examination of newborn revealed multiple tiny clear vesicular eruptions that closely mimicked sprinkled water droplets [Figure 1] and [Figure 2]. The lesions were about 1-3 mm size, seen predominantly over the neck, upper chest, back, and both upper limbs. The lesions were closely placed (in crops) with a shiny surface. The underlying skin was normal, without any evidence of erythema or induration. The lesions ruptured easily but healed without leaving any marks. The baby was otherwise active and feeding well. Vitals and systemic examination were normal. A diagnosis of miliaria crystallina (MC) was considered based on the morphology of the lesions. No new lesions appeared after 1 st day. The lesions disappeared spontaneously within the first 4 days of life.
|Figure 1: Picture taken immediately after birth (note the moist and fleshy umbilical cord stump) showing distribution of vesicles involving the trunk and the upper extremities|
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|Figure 2: Tiny, clear, vesicular eruption mimicking sprinkled water droplets in upper extremity|
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Miliaria crystallina is a transient, self-limiting, superficial obstruction of eccrine sweat ducts resulting in extravasation of sweat into epidermis. MC may present in the neonatal period but congenital occurrence is extremely rare.  This benign self-limiting condition is often triggered by hot and humid climate. The lesions contain clear watery fluid, thin-roofed, and without any inflammation. The lesions are generalized involving face, trunk and extremities but palms, soles, and mucosa are usually spared.  The risk factors for developing congenital MC are maternal febrile illness prior to delivery, moist occlusive environment of amniotic fluid, and vernix caseosa.  The presence of maternal fever was the trigger for congenital MC lesions in our case. Aspiration cytology reveals clear serous fluid with no inflammatory cells or multinucleated giant cells. No therapy is required as this condition is self-limiting and resolves without any complications.
| References|| |
|1.||Babu TA, Sharmila V. Congenital miliaria crystallina in a term neonate born to a mother with chorioamnionitis. Pediatr Dermatol 2012;29:306-7. |
|2.||Taieb A, Boralevi F. Common transient neonatal dermatoses. In: Harper J, Oranje AP, Prose NS, editors. Textbook of Pediatric Dermatology. Oxford: Blackwell; 2006. p. 63-5. |
[Figure 1], [Figure 2]