Search Results - "BERTSCH, H. P"

Insect bite-like reactions in a patient with B-cell chronic lymphocytic leukaemia: fluorescence in situ hybridization analysis revealed neoplastic B cells within the skin infiltrate by Mitteldorf, C., Tronnier, M., Merz, H., Haenssle, H.A., Bertsch, H.P., Schön, M.P., Kaune, K.M.

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Progression of a CD4+ CD56+ blastic plasmacytoid DC neoplasm after initiation of extracorporeal photopheresis in an allogeneic transplant recipient by Dohm, A, Hasenkamp, J, Bertsch, H P, Maas, J H, Truemper, L, Wulf, G

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Sentinel lymphonodectomy does not increase the risk of loco-regional cutaneous metastases of malignant melanomas by Kretschmer, L., Beckmann, I., Thoms, K.M., Haenssle, H., Bertsch, H.P., Neumann, Ch

“…With regard to malignant melanoma, the impact of lymph node surgery on the development of loco-regional cutaneous metastases (LCM) has not yet been adequately…”
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Successful treatment of classic Kaposi sarcoma with low-dose intramuscular immunoglobulins by Thoms, K.-M., Hellriegel, S., Krone, B., Beckmann, I., Ritter, K., Schön, M. P., Bertsch, H. P., Kretschmer, L.

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Folliculotropic mycosis fungoides with CD30+ large-cell transformation in a young woman: beneficial effect of bexarotene by Mitteldorf, C., Stadler, R., Bertsch, H.P., Neumann, C.

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Acroangiodermatitis Mali resulting from arteriovenous malformation: report of a case of Stewart-Bluefarb syndrome by Zutt, M., Emmert, S., Moussa, I., Haas, E., Mitteldorf, C., Bertsch, H. P., Neumann, C.

“…Summary We describe the rare Stewart–Bluefarb syndrome in a 15‐year‐old boy. This syndrome presents as a congenital arteriovenous malformation of the lower leg…”
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Papular exanthem discloses acute myeloid leukaemia: interphase fluorescence in situ hybridization revealed deletion of p53 and gain at 8q22/8q24/Tel8q without trisomy 8 by Kaune, K. M., Baumgart, M., Schmitke, E., Haase, D., Middel, P., Ghadimi, B. M., Bertsch, H. P., Neumann, C., Emmert, S.

“…Summary We describe a 79‐year‐old patient who presented with fatigue, weight loss, pancytopenia and a papular exanthem. Previous attempts to taking bone‐marrow…”
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CD4+ CD56+ blastic tumor of the skin: cytogenetic observations and further evidence of an origin from plasmocytoid dendritic cells by HALLERMANN, C, MIDDEL, P, GRIESINGER, F, GUNAWAN, B, BERTSCH, H. P, NEUMANN, C

“…We here report on a case of a blastic tumor, recently described to belong to a new entity sharing phenotypic similarities with blood derived plasmocytoid…”
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Extracorporeal photochemotherapy for the treatment of exanthematic pityriasis rubra pilaris by Haenssle, H. A., Bertsch, H. P., Emmert, S., Wolf, C., Zutt, M.

“…Summary Pityriasis rubra pilaris (PRP) is a rare papulosquamous skin disease of unknown aetiology that has been categorized into five clinical types based on…”
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Results of a surveillance programme for patients at high risk of malignant melanoma using digital and conventional dermoscopy by Haenssle, H A, Vente, C, Bertsch, H P, Rupprecht, R, Abuzahra, F, Junghans, V, Ellinghaus, B, Emmert, S, Hallermann, C, Rosenberger, A, Neumann, C

“…Patients with a high number of atypical naevi and a personal and/or family history of melanoma are at high risk of malignant melanoma. The objective of this…”
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Bexarotene does not prevent secondary Hodgkin's lymphoma in mycosis fungoides by Mitteldorf, C, Bertsch, HP, Kaune, KM, Krüger, U, Klemke, C-D, Neumann, C

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High incidence of in-transit metastases after sentinel node biopsy in patients with melanoma (Br J Surg 2004; 91: 1370-1371) by Kretschmer, L., Beckmann, I., Thoms, K. M., Haenssle, H., Bertsch, H. P., Neumann, Ch

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Lacking CD56 expression in a relapsing cutaneous blastic plasmacytoid dendritic cell neoplasm after allogeneic bone marrow transplantation: FISH analysis revealed loss of 11q by Mitteldorf, C., Bertsch, H.P., Baumgart, M., Haase, D., Wulf, G., Schön, M.P., Rosenwald, A., Neumann, C., Kaune, K.M.

“…Background  Blastic plasmacytoid dendritic cell neoplasm (BPDCN) is a rare entity characterized by a CD4+/CD56+/CD123+ immunophenotype and a fatal clinical…”
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Ki-S1 and PCNA expression in erythroid precursors and megakaryocytes--a comparative study on proliferative and endoreduplicative activity in reactive and neoplastic bone marrow lesions by Thiele, J, Bertsch, H P, Kracht, L W, Anwander, T, Zimmer, J D, Kreipe, H, Fischer, R

“…The monoclonal antibody Ki-S1 reacts with a cell proliferation-associated nuclear antigen which is expressed in the G1 through G2/M phases of the cell cycle…”
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Therapie des Granuloma anulare disseminatum mit Anthralin by Jantke, M.E., Bertsch, H.-P., Schön, M.P., Fuchs, T.

“…Zusammenfassung Das Granuloma anulare ist eine gutartige, häufig asymptomatische und selbstlimitierende granulomatöse Hauterkrankung. Beim disseminierten…”
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Follicular mycosis fungoides. A histopathologic analysis of nine cases by Flaig, Michael J., Cerroni, Lorenzo, Schuhmann, Kathrin, Bertsch, Hans Peter, Kind, Peter, Kaudewitz, Peter, Sander, Christian A.

“…Background: The spectrum of mycosis fungoides is exceedingly broad. Many different variants have been described, based on both clinical appearance and…”
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Splenic megakaryocytopoiesis in primary (idiopathic) osteomyelofibrosis. An immunohistological and morphometric study with comparison of corresponding bone marrow features by Thiele, J, Klein, H, Falk, S, Bertsch, H P, Fischer, R, Stutte, H J

“…An immunohistochemical and morphometric study has been performed on splenic tissue of 10 patients with primary (idiopathic) osteomyelofibrosis (OMF) to…”
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Uncommon cutaneous ulcerative and systemic sarcoidosis. Successful treatment with hydroxychloroquine and compression therapy by Meyersburg, D, Schön, M P, Bertsch, H P, Seitz, C S

“…Sarcoidosis is a granulomatous multisystemic disease of unclear etiology, which can affect any organ. The cutaneous manifestations are variable, but ulcerative…”
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Treatment of disseminated granuloma annulare with anthralin by Jantke, M E, Bertsch, H-P, Schön, M P, Fuchs, T

“…Granuloma annulare is a benign, often asymptomatic and self-limiting granulomatous skin disease. In cases of disseminated granuloma annulare, spontaneous…”
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Myelodysplastic syndromes: immunohistochemical and morphometric evaluation of proliferative activity in erythropoiesis and endoreduplicative capacity of megakaryocytes by Thiele, J, Hoffmann, I, Bertsch, H P, Fischer, R

“…An immunohistochemical and morphometric analysis was performed on bone marrow trephine biopsies in 40 patients with primary myelodysplastic syndromes (MDS) to…”
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