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Titlebook: Deadly Dermatologic Diseases; Clinicopathologic At Michael B. Morgan,Bruce R. Smoller,Stephen C. Soma Book 20071st edition Springer-Verlag

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https://doi.org/10.1007/978-3-031-55098-0ance is similar to that of cutis laxa. This extremely rare variant of mycosis fungoides affects middle-aged adults with a slight predilection for women in some, but not all, series (2–5). It is most common in Caucasians.
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Cutaneous B-Cell Lymphomahese patients in order to determine the extent of disease. The prognosis is greatly altered depending upon this extent. As subtypes of lymphoma correlate with clinical correlation, histologic findings, and prognosis, several of the most prevalent subtypes will be described individually.
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Langerhans Cell Histiocytosis of Birbeck granules as a specific ultrastructural marker for Langerhans cells (3), the infiltrating cells of histiocytosis X were identified as Langerhans cells. In 1987, the Writing Group of the Histiocyte Society proposed that . replace the term . as more appropriate (4).
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Paget’s Diseasetics as breast carcinoma, independent of the presence of Paget’s disease. It is most frequently encountered in middle-aged to elderly women and it may be unilateral or bilateral. Mammary Paget’s disease presents as an erythematous, scaling patch on the nipple (Figure 9.1).
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Angiosarcomalium that occurs in a variety of anatomic sites including the skin (1–3). Sixty percent of cases arise within the skin or superficial soft tissues. Although these tumors derive from the vascular endothelium, the exact vascular origin is unknown and likely derives from both the blood vessels and lymp
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