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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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Cowden’s Syndromeneck, as exophytic, small, hyperkeratotic papules (Figure 15.1). There is no particular gender predilection and they usually arise during the second decade. When occurring as isolated lesions, these tumors are invariably benign and are of no clinical significance.
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Muir-Torre Syndromest cases, these lesions are less than 1 cm in diameter (1). While they may occur at any body site, they are most common on the face. They usually appear in middle age. Ulceration is not a common feature.
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Amyloidosis: Systemic, Nodular, and Epidermal Derived defined by certain histomorphologic and chemical properties that permit their identification and inclusion into disease categories (1). These designations can be loosely grouped into systemic and cutaneous delimited forms.
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Gyrate Erythemas: Erythema Gyratum Repens and Erythema Chronicum Migranserythema marginatum rheumaticum (EMR), erythema gyratum repens (EGR), and erythema chronicum migrans (ECM). The latter two entities, namely EGR and ECM, are associated with potentially deadly underlying disorders and thus will be discussed in greater detail.
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Daniela D. Doneva,Stoytcho S. Yazadjiev 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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https://doi.org/10.1007/978-3-031-51093-9mic involvement (1,2). However, for the sake of completeness, the other variants of this disease spectrum will also be considered. Urticaria pigmentosa is the global term for all conditions that are characterized by increased numbers of mast cells within the dermis. There is no gender predilection.
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