fig 2 dermoscopy
Elena Thomaidou, et al. Two cases of disseminated superficial actinic porokeratosis (DSAP) and treatment literature review
Sarra Harbaoui, et al. Multiple and giant perforating pilomatrixoma: a case report
Mrinal Gupta. Epithelioma cuniculatum arising on a preexisting wart
Guneet Awal, et al. Stewart Bluefarb syndrome: case report of a rare variant of acroangiodermatitis
Taghreed Mahjoub. Unilateral nevoid hyperkeratosis of the nipple and areola in a Saudi female


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Conclusion: Our results have demonstrated the importance of determining IFN-g concentrations in serum in patients with AU. This research could contribute to the interpretation of insufficiently well known views of the pathogenesis role and significance of IFN-g in AU.

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In HIV infected patients with low CD4+ counts <200/cmm, on HAART, if skin lesions with numbness appearing within first six months of initiation of the treatment, a differential diagnosis of leprosy in the form of immune reconstitution inflammatory syndrome should be made with priority in high endemic areas. A wide variety of atypical clinical presentations and serious reactions should be anticipated. More systematic studies are required to understand the immune and inflammatory mechanisms associated with the condition.

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Many studies have demonstrated that DC is principally a disease of defective telomere maintenance. DC patients normally have very short telomeres, which could be related to the fact that some DC patients are reported to have mutations in different genes encoding components of the telomerase complex. Previous electron microscopy studies revealed that cells isolated from DC patients have an embryonic immature nucleus, which could induce malignant transformation. Cancer usually develops after the third decade; the most frequent solid malignancies are head and neck squamous cell carcinomas. Although we have not detected any malignant changes, we need to follow-up with this first case of DC in Vietnam regularly.

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