Proteus syndrome in Child
A plethora of clinical manifestations accompany Proteus syndrome and are variable between patients. Hemihyperplasia (asymmetric overgrowth of the head, face, digits, or limbs) is usually found. Overgrowth of the cranium, vertebrae, spleen, thymus, or external auditory meatus may occur. The presence of cerebriform connective tissue nevi is a characteristic finding, but these are not always present. Other cutaneous and soft tissue abnormalities include epidermal nevi, vascular malformations, pigmentary changes, and disordered adipose tissue growth leading to either lipomas or lipohypoplasia. Furthermore, a variety of skeletal, visceral, central nervous system (CNS), and ocular abnormalities may be present. Ovarian cystadenomas and parotid monomorphic adenomas are overrepresented in Proteus syndrome patients. A distinctive facial phenotype has been described in patients with intellectual impairment.
Some manifestations are usually present at birth, but this diagnosis may not be suspected until late infancy, depending upon the rate of overgrowth and appearance of skin lesions. Overgrowth progresses through childhood and then stabilizes.
Prognosis depends upon the severity of disease. Complications include respiratory compromise or cord compression from spinal defects, major deformity and disability, and increased risk of venous thrombosis and pulmonary embolism. Most patients have normal intelligence, but some have learning disabilities or seizures.
Q87.3 – Congenital malformation syndromes involving early overgrowth
23150001 – Proteus syndrome
- Klippel-Trenaunay syndrome – Has signs that are limited to one extremity.
- Neurofibromatosis – Typically has a family history. A physical examination or eye examination may help differentiate this diagnosis.
- Encephalocraniocutaneous lipomatosis
- Bannayan-Riley-Ruvalcaba syndrome – An autosomal dominant syndrome characterized by macrocephaly, multiple lipomas, and hemangiomata.
- Maffucci syndrome – Consists of enchondroma with multiple angiomas.