Search PubMed⌕ Search

Biomedical subjects

H Kresbach

Publications and source records attributed to H Kresbach.

At least 37 records · Page 2Linked to original sources

[Cutaneous malignant lymphomata. Older ideas and newer concepts (author's transl)].

The new interpretation of the classical clinical, histological and cytomorphological findings by means of modern methods has led to older ideas of cutaneous lymphoreticular neoplasias having to give way to newer concepts. Most of the earlier reticuloses are today to be considered as cutaneous B cell lymphomata. The rest are divided among cutaneous T cell lymphomata, leukemias and malignant histiocytic diseases. Lympohosarcomata are completely absorbed into the lymphoma concept, reticulosarcomata - as far as is known at present - are to be included partly among the giant cell blastic lymphomata and partly among diseases of the mononuclear phagocyte system. There appears no longer to be any place for a "reticulosis". The relatively large group of unclassified cutaneous lymphomata is perhaps a reminder to exercise care here.

Diagnosis, Differential↗

[Annotations on malignant cutaneous lymphomas].

The majority of the formerly called "malignant skin reticuloses" can now be classified as neoplasias of lymphatic cells. Still other cases belong to myeloproliferative diseases or to malignant disorders of the monocyte--histiocyte--macrophage system.

Histiocytes↗

[Genital bowenoid papulosis. Pseudo-Bowen's disease of the genital area].

This report deals with a new disease, which is characterized by multiple reddish papules on the genitalia of young adults. The histological picture shows changes of squamous cell carcinoma in situ. The possible etiology is discussed. It is too early to predict the biological behaviour of these lesions.

Adult↗

[The presence of scleroderma and chronic lymphadenosis concurrently in a patient (author's transl)].

This report deals with the case of a 50 year-old woman with long-standing scleroderma of the acral-asphyxial type with a relatively slight tendency to progression. Chronic lymphadenosis has been an additional feature of this case over the past few years. The following findings appear of particular interest: autoimmune phenomena in the form of antinuclear antibodies, a virtually monoclonal proliferation of B-lymphocytes and a relative T-lymphocyte deficiency. It is suggested that both conditions may be pathogenetically connected with an immunologically defined insufficiency of the lymphocytic system. Hence, in view of this observation, it may not be correct to consider scleroderma a "paraneoplastic phenomenon".

Antibody Formation↗