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S13-IMAGE MAP
The conventions for this section are the same as those for all the preceding sections: S=section, C=chapter, VA=visual aid, and P=pictorial. A click on an underlined item in the list below will take the reader to the
selected visual aid, or pictorial. The SECTION MAP provides a brief description of the basic reaction pattern that is discussed in each section. In the MASTERBORDER to the left, S-C- items are symbols for textual
chapters at level 2. An S-C- item with the suffix “-X” is a parent textual chapter for one or more pictorials at level 3. An S-C-P- item, or a S-C-VA- item is a pictorial, or a visual aid, respectively.
PHOTOMICROGRAPHS
S13C3P1-1-4: histiocytosis X; S13C4P2-1-6: histiocytosis X;
S13C4aP2a-1-6: atypical histiocytosis; S13C4bP2b-1-6: atypical histiocytosis;
S13C5P3-1-5: congenital histiocytosis; S13C6P4-1-3: congenital histiocytosis; S13C6bP4b-1-7: Letterer-Siwe disease;
S13C6aP4a-1-4: sinus histiocytosis; S13C6aP4a-5-7: multicentric reticulohistiocytosis;
S13C6bP4b-1-7: Letterer-Siwe disease;
S13C6cP4c-1-6: spongiotic and pagetoid histiocytosis;
S13C7P5-1-4: T-cell dysplasia; S13C7aP5a-1-6: T-cell dysplasia;
S13C8P6-1-5: lymphoproliferative disorder (lymphomatoid papulosis);
S13C9P7-1-5: lymphoproliferative disorder (pityriasis lichenoides-like variant);
S13C10P8-1-6: lymphoproliferative disorder (lymphomatoid papulosis, type A);
S13C10aP8a-1-4: lymphoproliferative disorder (lymphomatoid papulosis, type A); S13C10aP8a-5 & 6: atypical cutaneous lymphoplasia; S13C10bP8b-1-4: atypical cutaneous lymphoplasia;
S13C11P9-1-4: angioproliferative disorder (angiolymphoid hyperplasia with eosinophilia); S13C11aP9a-1: angiolymphoid hyperplasia with eosinophilia;
S13C12P10-1-4: lichenoid melanocytic dysplasia;
S13C13P11 -1-5: halo nevus variants;
S13C13aP11a-1-5: xeroderma pigmentosa; S13C13bP11b-1-7: xeroderma pigmentosa;
S13C14P12-1-5: porokeratosis;
S13C14aaP12aa-1-3: porokeratosis (psoriasiform cornoid lamella);
S13C14aP12a-1-6: Kaposi’s disease;
S13C14bP12b-1-5: Kaposi’s disease;
S13C15P13-1-3: Kaposi’s sarcoma (angiomatous variant;
S13C16P14-1-6: Kaposi’s disease-like, low-grade angiosarcoma);
S13C17P15-1-7: Kaposi’s sarcoma; mixed fibrotic and solid patterns;
S13C18P16-1-6: Paget’s disease; S13C19P17-1-3: Paget’s disease;
S13C20P18-1-4: epithelioid sarcoma; S13C20P18-4: epithelioid sarcoma (large cell sarcoma of Bliss and Reed (gross specimen);
S13C21P19-1-3: atypical condyloma acuminatum;
S13C22P20-1-4: systemic mastocytosis;
S13C23P21-1-4: epidermodysplasia verruciformis;
S13C24P22-1-3: pseudoporphyria (drug-induced bullous photosensitivity to tetracyclines);
S13C24P22-4-6: acute pityriasis lichenoides (continued on S13C24aaP22aa);
S13C24aaP22aa-1 & 2: acute pityriasis lichenoides (component of transformed lymphoid cells -
mild T cell dysplasia of indeterminate type);
S13C24aP22a-1-6: herpes virus infection vs erythema multiforme;
SECTION MAP
Section 1: inflammation, general
Section 2: spongiotic & psoriasiform disorders
Section 3: lichen planus & LP-like disorders
Section 4: erythema multiforme-like & pityriasic disorders
Section 5: lupus erythematosus & LE-like disorders
Section 6: pemphigus & pemphigoids (1)
Section7: vesiculo-bullous disorders, misc. (2)
Section 8: vasculitides
Section 9: collagenoses (including scleroderma, mucinoses, and elastoses)
Section 10: panniculitides
Section 11: infections
Section 12: granulomas
Section 13: borderland
Section 14: clinical
Section 15: borderland2
Section 16: site diagram.
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