Indian Journal of Dermatology
E-IJD CORRESPONDENCE
Year
: 2016  |  Volume : 61  |  Issue : 2  |  Page : 239-

Hurler's disease with multiple atypical mongolian spots


Sidharth Sonthalia1, Rashmi Khurana2,  
1 Department of Dermatology, Skinnocence Skin Clinic, Haryana, Gurgaon, India
2 Department of Dermatology, Kalyani-Escorts Hospital, Haryana, Gurgaon, India

Correspondence Address:
Sidharth Sonthalia
Department of Dermatology, Skinnocence Skin Clinic, Haryana, Gurgaon
India




How to cite this article:
Sonthalia S, Khurana R. Hurler's disease with multiple atypical mongolian spots.Indian J Dermatol 2016;61:239-239


How to cite this URL:
Sonthalia S, Khurana R. Hurler's disease with multiple atypical mongolian spots. Indian J Dermatol [serial online] 2016 [cited 2021 Nov 28 ];61:239-239
Available from: https://www.e-ijd.org/text.asp?2016/61/2/239/177795


Full Text

Sir,

Extensive and abnormal presentations of birthmarks are often a clue to an underlying systemic disorder. We report the case of a 3-day-old neonate, in whom such a presentation resulted in the diagnosis of an inborn error of metabolism (IEM). The neonate delivered full term and vaginally, presented with multiple round-to-ovoid bluish noninfiltrated macules over the lower back, buttocks, thighs and left scapula, suggestive of extensive and aberrant Mongolian spots (MSs) [Figure 1]. A small dark bluish-black macule was evident within the large MS over the right lower back (“MS within MS”). Facial examination revealed multiple erythematous macules over the eyelids and pinnae, suggestive of salmon patches [Figure 2]. Further examination revealed normal anthropometry with the absence of facial dysmorphism. There was no history of seizures. Muscle tone and reflexes were preserved. There was no hepatosplenomegaly. Perinatal and family histories were insignificant with no consanguinity in parents. Ophthalmological and neurological evaluations were normal. Histopathology from scapular lesion revealed the presence of melanin-loaded fusiform melanocytes in mid-to-lower dermis, scattered between collagen bundles, consistent with MS. Skeletal radiographs of the skull, spine and limbs, abdominal ultrasound and computed tomography of the brain were unremarkable. Peripheral blood smear revealed vacuolated lymphocytes. Urinalysis for glycosaminoglycans confirmed mucopolysacchariduria. The enzyme α-L-iduronidase was undetectable in plasma on enzyme assay, confirming the diagnosis of Hurler's disease. The child was referred to a clinical geneticist for genetic evaluation and treatment with enzyme replacement therapy.{Figure 1}{Figure 2}

MSs are bluish-black birthmarks over the gluteal region, more commonly encountered in African or Asian population. Although spontaneous lightening is expected, atypical presentations of MS are markers of persistence and often suggest an underlying IEM [1],[2] Atypical MS includes (1) multiple and extensive MS, (2) extrasacral or “aberrant” MS, (3) deeply pigmented MS, and (4) “MS within MS.” The IEMs typically associated with atypical MS are mucopolysaccharidosis (MPS), most commonly MPS-I or Hurler's disease followed by GM1 gangliosidosis.[2],[3]

Children with MPS often have no clinical signs at birth. Features typical of MPS such as dysmorphic facies, skeletal dysplasia, ocular abnormalities, hepatosplenomegaly, developmental delay and neuromuscular deficits appear in the first 6–12 months. Vacuolation of lymphocytes on peripheral smear and mucopolysacchariduria are suggestive, and deficient blood levels of lysosomal enzymes are confirmatory.[4] Targeted mutation analysis of IDUA gene is needed for confirmation of the diagnosis of Hurler's syndrome and detection of familial carriers, respectively. Ancillary evaluation for systemic involvement is essential in an established case.

Despite this neonate not having any clinically apparent signs of Hurler's Syndrome, laboratory results confirmed it. Since atypical MS is now a well-established cutaneous marker of underlying MPS, this report reiterates the significance of such association. This is also the first report of such an association from India. Although this child had additional salmon patches, it is premature to comment on the additional significance of the presence of these vascular birthmarks. Since MPS-associated irreversible organ damage is preventable only by early administration of enzyme replacement and/or other therapies, recognition of cutaneous markers like atypical MS may prove to be life-saving for such children.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

References

1Gupta D, Thappa DM. Mongolian spots: How important are they? World J Clin Cases 2013;1:230-2.
2Hanson M, Lupski JR, Hicks J, Metry D. Association of dermal melanocytosis with lysosomal storage disease: Clinical features and hypotheses regarding pathogenesis. Arch Dermatol 2003;139:916-20.
3Rybojad M, Moraillon I, Ogier de Baulny H, Prigent F, Morel P. Extensive Mongolian spot related to Hurler disease. Ann Dermatol Venereol 1999;126:35-7.
4Wraith JE. Mucopolysaccharidoses and mucolipidoses. Handb Clin Neurol 2013;113:1723-9.