LEADER 07334nam 22006135 450 001 9910484995503321 005 20251113210034.0 010 $a3-030-59129-8 024 7 $a10.1007/978-3-030-59129-8 035 $a(CKB)5590000000442443 035 $a(MiAaPQ)EBC6533360 035 $a(Au-PeEL)EBL6533360 035 $a(OCoLC)1245672085 035 $a(PPN)254724892 035 $a(DE-He213)978-3-030-59129-8 035 $a(EXLCZ)995590000000442443 100 $a20210331d2021 u| 0 101 0 $aeng 135 $aurcnu|||||||| 181 $ctxt$2rdacontent 182 $cc$2rdamedia 183 $acr$2rdacarrier 200 10$aCutaneous Lymphomas $eUnusual Cases 3 /$fedited by Oleg E. Akilov 205 $a1st ed. 2021. 210 1$aCham :$cSpringer International Publishing :$cImprint: Springer,$d2021. 215 $a1 online resource (132 pages) $cillustrations 225 1 $aMedicine Series 311 08$a3-030-59128-X 320 $aIncludes bibliographical references. 327 $aCase 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 posttransplant lymphoproliferative disorder with ? expression -- Case 44. Primary cutaneous marginal zone lymphoma presented as facial patches unresponsive to rituximab -- Case 45. Primary cutaneous diffuse large B-cell lymphoma, leg type presenting on the scalp -- Case 46. Bruise-like nodules of blastic plasmacytoid dendritic cell neoplasm on the background of diffuse petechiae -- Case 47: Blastic plasmacytoid dendritic cell neoplasm presented with deep purple nodules -- Case 48: A solitary nodule of blastic plasmacytoid dendritic cell neoplasm in a young patient -- Case 49. A relapse of T-cell large granular lymphocytic (LGL) leukemia with chronic NK lymphocytosis in the skin -- Case 50. Indeterminate dendritic cell histiocytosis -- Case 51. A unique presentation of hemophagocytic lymphohistiocytosis with ulcerating papulonodules. 330 $aThis book provides a current experience in the diagnostic diagnostic techniques and treatment approaches available for unusual cutaneous lymphomas. It features concise case-based chapters with a particular emphasis on instances of mature T-cell and NK-cell neoplasms, mature B-cell neoplasms, immature hematopoietic malignancies, and other lymphoproliferative disorders. Clinically-oriented cases emphasize the importance of physical examination along with modern tests of laboratory diagnostics and clinico-pathological correlations. Cutaneous Lymphomas: Unusual Cases 3 presents a range of difficult and rare cases, which would be uncommon even to the specialists in this field. Therefore, it is a vital reference source for dermatologists, dermatophatologists, cutaneous oncologists, hematooncologists, pathologists, oncologists, and other medical professionals who treat these patients. 410 0$aMedicine Series 606 $aDermatology 606 $aPathology 606 $aOncology 606 $aDermatology 606 $aPathology 606 $aOncology 615 0$aDermatology. 615 0$aPathology. 615 0$aOncology. 615 14$aDermatology. 615 24$aPathology. 615 24$aOncology. 676 $a616.99446 676 $a616.99446 702 $aOleg E. Akilov 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910484995503321 996 $aCutaneous lymphomas$92855496 997 $aUNINA