Olmsted Sydrome Accompanıed by Immune Deficiency
Journal Title: Scholars Journal of Medical Case Reports - Year 2013, Vol 1, Issue 1
Abstract
Olmsted Syndrome, OS, ( congenital palmoplanter and periofical karetoderma) is a very rare condition and is associated with palmoplanter karetoderma and perioral hyperkaratotic plaques, deformation and loss of the flexibility of hands. On rare occasions it could lead to amputation of the severely effected digits or hands. The condition has also been associated with growth impairement and joint laxity and described to be inherited from the famility or effect patients sporadicaly. Specific types of skin lesions are formed with OS. New types of leasions and plaques are still being identified with new patients. In our sunjest we have seen depletion of IgG2 levels (immune deficiency) severe pneumonia and empyema during skin deformation. Although all reported cases have been described to have genetic links or appear sporadicly, our findings show that the depletion of the immune responses should also be considered and not ignored when identifying and diagnosing the condition. Keywords: Olmsted syndrome, Child, immune deficiency
Authors and Affiliations
Fatih Kılıçbay, Hatice Sağlam Fitöz, Derya Yayla, Turan Yıldız, Zekeriya İlçe
Collision Tumor of Ovary: Invasive Serous Papillary Cystadenocarcinoma and Mature Cystic Teratoma
Collision tumour is defined as coexistence of two dintinct tumours in the same organ without any histological intermixing. Collision tumors involving ovaries are extremely rare. In this paper, we present a case of ovaria...
Granulomatous mastitis masquerading as breast carcinoma
Granulomatous mastitis is a rare inflammatory disease of the breast with no known etiology. It presents most commonly with a palpable mass and erythematous skin. Often, the initial diagnosis offered clinically is breast...
Staphylococcal Scalded Skin Syndrome –A Case Report
Staphylococcal scalded skin syndrome is caused by staphylococcus aureus. An exfoliative toxin A being responsible for the causes of the disease. This disease usually affects neonates and generally responds rapidly to ant...
Meckel Gruber Syndrome-An Autopsy Report of a Rare Case
Abstract:Meckel Gruber Syndrome is a rare autosomal recessive disorder characterized by a typical clinical triad of meningo-encephalocele, polycystic kidneys and polydactyly. The worldwide incidence varies from 1 in 1325...
Chronic Suppurative Osteomyelitis of the Mandible: Case Report and Review.
Osteomyelitis is a challenging disease for clinicians and patients despite the many advances in diagnosis and treatment. Chronic suppurative osteomyelitis (CSO) of the mandible is often considered difficult to treat. Se...