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Case 1: Folliculotropic mycosis fungoides with central nervous system involvement.- Case 2: Erythema gyratum repens-like mycosis fungoides with large cell transformation.- Case 3: Eczema molluscatum in a patient with erythrodermic mycosis fungoides.- Case 4: Parakeratosis variegata-like poikilodermatous CD8+ mycosis fungoides.- Case 5: Parakeratosis variegata in a patient with CD8+ mycosis fungoides with post-inflammatory hypopigmentation.- Case 6: Poikilodermatous mycosis fungoides.- Case 7: Tumor mycosis fungoides with xanthomatized atypical lymphocytes.- Case 8: CD20+ mycosis fungoides partially responsive to rituximab.- Case 9: Chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids (CLIPPERS) in a patient with granulomatous mycosis fungoides and multiple tumors.- Case 10. Folliculotropic mycosis fungoides with exuberant neutrophil-rich scale and follicular plugging mimicking hypertrophic actinic keratosis.- Case 11. Small plaque parapsoriasis-like mycosis fungoides.- Case 12. Extragenital lichen sclerosus et atrophicans mimicking hypopigmented mycosis fungoides.- Case 13: T-cell-rich angiomatoid polypoid pseudloymphoma (TRAPP) of the skin.- Case 14. Pustular Sezary syndrome.- Case 15. De novo expression of CD26 on Sezary cells as an indicator of the disease progression in a patient with Sezary syndrome.- Case 16. Sezary syndrome presenting with papuloerythroderma of Ofuji and leonine facies.- Case 17. Mycosis fungoides-like presentation of primary cutaneous anaplastic large cell lymphoma.- Case 18. Anaplastic lymphoma kinase-positive primary cutaneous anaplastic large cell lymphoma.- Case 19. Successful treatment of primary cutaneous anaplastic large cell lymphoma on the penile shaft with brentuximab vedotin and allogenic stem cell transplant.- Case 20. Lymphomatoid papulosis type D in a child with CD8+ hypopigmented mycosis fungoides.- Case 21. Lymphomatoid papulosis and autoimmunity.- Case 22. Infusion-related CD30-positive lymphomatoid drug eruption secondary to melphalan.- Case 23. Arthropod reaction with CD30 positive infiltrate and ulceration mimicking CD30 lymphoproliferative disorder.- Case 24: Extranodal NK/T-cell lymphoma, nasal type.- Case 25. EBV-associated extranodal NK/T-cell lymphoma with ?/? TCR expression presented as aphthous stomatitis.- Case 26. Extranodal NK/T-cell lymphoma, extra-nasal type.- Case 27: Disseminated extranodal NK/T-cell lymphoma.- Case 28. Primary cutaneous ?? T-cell lymphoma with mycosis fungoides-like plaques.- Case 29. Indolent primary cutaneous ?? T-cell lymphoma mimicking mycosis fungoides.- Case 30. Primary cutaneous ?? T-cell lymphoma with poor response to the therapy.- Case 31. Primary cutaneous unilateral non-cytotoxic ?? T-cell lymphoma slowly progressing into tumors.- Case 32. Primary cutaneous ?? T cell lymphoma with panniculitis-like presentation.- Case 33: Primary cutaneous aggressive epidermotropic CD8-positive T-cell lymphoma with initial protracted course.- Case 34. Primary cutaneous aggressive epidermotropic T-cell lymphoma (PC-AETCL) with an aberrant immune phenotype.- Case 35. CD8+ T-cell lymphoma with cytotoxic phenotype.- Case 36. Primary cutaneous aggressive epidermotropic T-cell lymphoma as a composite lymphoma with B-cell chronic lymphocytic leukemia.- Case 37: Primary cutaneous aggressive epidermotropic CD8+ cytotoxic T-cell lymphoma with bullous manifestation.- Case 38. Leukemoid reaction mimicking aggressive epidermotropic CD8+ T-cell lymphoma.- Case 39. Cutaneous relapse of peripheral T-cell lymphoma, NOS by extension.- Case 40. Generalized lymphadenopathy and poikiloderma due to prolonged interferon-?-1b therapy misdiagnosed as peripheral T-cell lymphoma.- Case 41: Adult T-Cell Leukemia/Lymphoma.- Case 42. Cutaneous Epstein-Barr Virus post-transplant lymphoproliferative disorder.- Case 43. Primary cutaneous CD30 T-cell p

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