Hanna Cisoń, et al. Disseminated eczema or CTCL: Usefulness of high-frequency ultrasonography in the assessment of skin lesions of cutaneous T-cell lymphoma
Insaf Moubine, et al. Ibrutinib-induced pyoderma gangrenosum in a patient with chronic lymphocytic leukemia
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Hanna Cisoń, et al. Usefulness of ultrasonography in assessment of skin lesions of cutaneous T-cell lymphoma

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Conclusion: CL is an endemic disease in Al-Ramadi and represents a public health problem. A high rate of infection was recorded alongside the Euphrates River, especially the rural district, while it was low in the urban side of the city. Any parts of the city may be affected, yet Albu-Ali Jassim, Al-Tamim, Al-Sufia, and Al-Thalia were the most frequently involved regions of the city.

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Epidemiological, clinical, and etiological aspects and management of chronic ulcers at the University Hospital Center of Dermatology in Bamako, Mali

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Conclusion: At the end of our case study, it was clear that patient neglect or ignorance and the inadequacy of healthcare services were factors that had led the initial lesions to evolve into chronicity. Any ulceration of the lower limbs should be taken seriously by patients, healthcare professionals, and health authorities. Furthermore, chronic leg ulcers should receive early intervention to prevent dramatic complications.

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DRESS syndrome and liver involvement: A study of 72 patients

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Conclusion: Hepatic involvement is common in DRESS syndrome, predominantly manifesting as cytolytic or cholestatic patterns. Maculopapular rash and erythroderma are the most commonly observed cutaneous phenotypes. These patients are more likely to have associated renal involvement and eosinophilia. Allopurinol, neuroleptics, and Salazopyrin are the most frequently implicated drugs.

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Cutaneous leishmaniasis in Senegal: When the practitioner is disarmed

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A peculiar in situ case of cutaneous leukocytoclastic vasculitis induced by urinary infection

Ana Maria Abreu Velez, Bruce R. Smoller, Michael S. Howard

Conclusion: Cutaneous leukocytoclastic vasculitis (LCV) is a disease thought to be related to the presence of immune complex deposition within small blood vessel walls. A 58-year-old female presented with purpuric papules on both legs, occurring concurrent with urinary symptoms. Histologically, an intraepidermal blister with luminal fragmented neutrophils was present. A dermal infiltrate was observed surrounding blood vessels; mild perivascular leukocytoclastic debris favored a diagnosis of LCV. Both direct immunofluorescence and immunohistochemistry staining also favored a diagnosis of LCV. Reactivity of the involved vessels was observed to multiple antibodies and complement, with overexpression of von Willebrand factor, CD15, and CD45. The ribosomal protein Phospho-S6 was also detected within the involved vessels, and on the blister roof and floor. The clinical triggering factor was a urinary infection that had progressed to urosepsis; the symptoms were effectively treated. We present an unusual case, where multiple immune reactions correlate with clinical and histologic changes characteristic of LCV.

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