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Year : 2019  |  Volume : 85  |  Issue : 5  |  Page : 509-511

Urticaria pigmentosa in monochorionic twins

Goknur Ozaydin Yavuz1, Ibrahim Halil Yavuz1, Serap Gunes Bilgili1, Remzi Erten2, Hulya Savas1, Irfan Bayram2,  
1 Department of Dermatology, Faculty of Medicine, Van Yuzuncu Yil University, Van, Turkey
2 Department of Pathology, Faculty of Medicine, Van Yuzuncu Yil University, Van, Turkey

Correspondence Address:
Dr. Serap Gunes Bilgili
Department of Dermatology, Faculty of Medicine, Van Yuzuncu Yil University, Van

How to cite this article:
Yavuz GO, Yavuz IH, Bilgili SG, Erten R, Savas H, Bayram I. Urticaria pigmentosa in monochorionic twins.Indian J Dermatol Venereol Leprol 2019;85:509-511

How to cite this URL:
Yavuz GO, Yavuz IH, Bilgili SG, Erten R, Savas H, Bayram I. Urticaria pigmentosa in monochorionic twins. Indian J Dermatol Venereol Leprol [serial online] 2019 [cited 2020 Sep 20 ];85:509-511
Available from: http://www.ijdvl.com/text.asp?2019/85/5/509/264007

Full Text


Mastocytosis is a rare clonal disease of the hematopoietic stem cells characterized by accumulation and proliferation of mast cells.[1] The disease manifests itself either as cutaneous mastocytosis affecting only the skin, or as systemic mastocytosis affecting multiple organs.[2] The abnormal accumulation of mast cells is mostly seen on the skin. The World Health Organization currently recognizes three main subforms of cutaneous mastocytosis: maculopapular cutaneous mastocytosis = urticaria pigmentosa, diffuse cutaneous mastocytosis and the mastocytoma of skin.[3],[4] According to the EU/US consensus group, maculopapular cutaneous mastocytosis can be divided into two variants: monomorphic maculopapular cutaneous mastocytosis and polymorphic maculopapular cutaneous mastocytosis.[5]

Familial cutaneous mastocytosis is rare and about 100 familial cases were reported until 2018, of which, at least 10 were monozygotic twins.[6],[7]

A pair of ten-month-old female monochorionic twins were admitted to our clinic (Department of Dermatology, Van Yuzuncu Yil University, Faculty of Medicine, Van, Turkey) with skin eruptions seen predominantly on the trunk, face and extremities. Their history revealed that the skin eruptions were present at birth and were given no treatment. No itching, flushing, diarrhea or syncope was reported.

Dermatological examination of the twins revealed yellow-tan, reddish-brown plaques on the extremities and bullae overlying some of the plaques [Figure 1]. Although Darier's sign was positive in both infants, they showed no signs of hepatosplenomegaly, lymphadenopathy or edema. Skin biopsy revealed a diffuse infiltrate of mast cells in the upper dermis with hematoxylin–eosin stain. CD117 staining was positive and toluidine blue stain confirmed the diagnosis [Figure 2], [Figure 3], [Figure 4]. The patients were referred to the pediatric out-patient clinic for looking into systemic involvement.{Figure 1}{Figure 2}{Figure 3}{Figure 4}

A complete blood cell count and biochemical profiles were within normal limits. For systemic involvement, abdominopelvic ultrasonography, trans-fontanel ultrasonography, chest radiography and cerebral magnetic resonance imaging were performed; all revealed normal findings. Patients were diagnosed as urticaria pigmentosa based on the clinical and histopathological findings. The patients were not started on any medications as they had only skin findings; however, they were placed on regular follow-up.

Mastocytosis, a disease characterized by clonal proliferation of mast cells in one or multiple organs, may lead to various clinical manifestations. Mastocytosis is defined in two main forms: cutaneous mastocytosis (involvement of skin alone) and systemic mastocytosis with involvement of the organs such as the liver, spleen and/or bone marrow.[2],[3],[6]

Cutaneous mastocytosis is a very rare disease that usually occurs sporadically. The prevalence of the cutaneous form has been reported with variations. Kiszewski et al. reported a prevalence of 1 in 500.[1] Familial cutaneous mastocytosis is rare and about 100 familial cases were reported until 2018, at least 10 of these cases were monozygotic twins.[4],[7] Urticaria pigmentosa, the most common form of cutaneous mastocytosis, also known as maculopapular cutaneous mastocytosis, is mainly seen in children. The lesions may be present at birth and often develop from early infancy to the age of two. Ben-Amitai et al. have demonstrated that the lesions of urticaria pigmentosa are present at birth in 20% of the pediatric cases of cutaneous mastocytosis and the majority of the lesions usually develop during the first year of life.[2] In our case, the lesions were congenital.

The typical presentation of urticaria pigmentosa is with yellow-tan to reddish-brown macules or slightly raised papules scattered mainly on the trunk and legs with generally less involvement of the sun-exposed areas. The disease generally spreads to palms, soles, face and scalp, especially in adults. Dermatologic symptoms are pruritus, “flushing” and “bullae.” Bullae formation is almost uniquely seen in children.[2],[6] In our case, yellow-tan to reddish-brown plaques on face, trunk and extremities and some bullae were noted in both of the twins. Erythema and urticarial wheals induced by physical trauma (e.g., rubbing, friction) is known as Darier's sign,[8] which was positive in our case.

Since the course of the disease is benign, the main objective of the therapy is to reduce the release of mast cell mediators and to inhibit their effects, thereby controlling signs and symptoms. Patients with urticaria pigmentosa and the families should be informed that they should avoid hot baths, sudden temperature changes, physical stimulants, vigorous rubbing of the skin, anxiety and drugs including aspirin, codeine, opiates, alcohol and radiocontrast substances containing iodide, to prevent exacerbations.[4],[8]

Childhood cases of urticaria pigmentosa have a good prognosis; systemic involvement is rare and usually spontaneously resolves until puberty.[4] In our case, physical examination, laboratory and radiological examinations showed no evidence of systemic involvement.

Finally, although familial cases of urticaria pigmentosa, diffuse cutaneous mastocytosis and mastocytomas have been reported, to our knowledge, this is the first report of urticaria pigmentosa seen in twins at the same time, which suggests that this form of mastocytosis is also genetically determined.[6],[9],[10],[11]

Declaration of patient consent

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

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Conflicts of interest

There are no conflicts of interest.


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8Güneş Bilgili S, Karadaǧ AS, Takci Z, Çalka Ö, Kösem M. Comparison of cutaneous mastocytosis with onset in children and adults. Turk J Med Sci 2014;44:504-10.
9Cainelli T, Marchesi L, Pasquali F, Rozzoni M. Monozygotic twins discordant for cutaneous mastocytosis. Arch Dermatol 1983;119:1021-2.
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