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Dive into the research topics where S. C. J. van der Putte is active.

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Featured researches published by S. C. J. van der Putte.


Histopathology | 1993

Cutaneous immunocytomas: a clinicopathologic study of 26 cases

J.U. Rijlaarsdam; S. C. J. van der Putte; Emilio Berti; H. Kerl; E. Rieger; J. Toonstra; Marie-Louise Geerts; C.J.L.M. Meijer; Rein Willemze

The clinical and histological features of 16 patients with a primary cutaneous immunocytoma and 10 patients with a secondary cutaneous immunocytoma are reported. In all cases the diagnosis was based on the presence of monotypic plasma cells or lymphoplasmacytoid cells. Our data show that primary cutaneous immunocytomas are a distinct type of cutaneous lymphoma, characterized by (a) the presence of solitary or localized skin lesions (13 of 16 cases); (b) preferential localization on arms and legs (15 of 16 cases); (c) excellent response to local treatment (15 of 16 cases) and (d) a favourable prognosis. Histologically, these primary cutaneous immunocytomas are characterized by the presence of nodular or diffuse infiltrates with monotypic lymphoplasmacytoid/plasma cells located at the periphery of the infiltrates. Important clinical and histological differences were noted between primary and secondary immunocytomas. In the latter group more widespread skin disease was seen, often in the presence of paraproteins and/or autoimmune diseases. In contrast with the peripheral localization of the monotypic cells in primary cutaneous immunocytomas the monotypic lymphoplasmacytoid/plasma cells in secondary immunocytomas formed diffuse infiltrates or these cells were found dispersed throughout the infiltrate. There were no differences in clinical presentation or course between the different subtypes of cutaneous immunocytomas (lymphoplasmacytic, lymphoplasmacytoid and polymorphic immunocytomas). The differential diagnosis between primary cutaneous immunocytomas and cutaneous plasmacytomas, primary follicular centre cell lymphomas and cutaneous ‘pseudolymphomas’ is discussed.


Cancer | 1985

A study to analyze the origin of tumor cells in malignant fibrous histiocytomas a multiparametric characterization

P. J. M. Roholl; J. Kleijne; C. D. H. van Basten; S. C. J. van der Putte; J. A. M. van Unnik

To study the derivation of tumor cells of malignant fibrous histiocytomas (MFH), their phenotypical marker profile was investigated and compared with those of malignant histiocytosis (MH) and of different types of soft tissue tumors (STT). The presence of the following markers was investigated: on paraffin sections, alpha‐1‐antichymotrypsin (ACT); on frozen sections antigens associated with lymphocytes, macrophages and fibroblasts, the enzymes acid phosphatase, nonspecific esterase, and beta‐glucuronidase; and, on isolated and cultured cells, the receptors for EA‐gamma and complement. Furthermore, the capacity to phagocytose sensitized erythrocytes and carbon particles was studied in vitro. MFH tumor cells and a part of other types of STT shared the expression of ACT and lysosomal enzymes with MH. They differed, however, from MH by the absence of monocyte/macrophage‐associated antigens and by the expression of fibroblast‐associated antigens, which property they had in common with other STT. MFH tumor cells were not able to form rosettes or to phagocytose Ig‐sensitized erythrocytes, but they showed phagocytosis of carbon particles. The results strongly indicate that MFH tumor cells originate from (primitive) fixed mesenchymal cells and are not related to monocyte‐derived histiocytes.


Archive | 1977

Lymphatic malformation in human fetuses

S. C. J. van der Putte

In 7 spontaneously aborted fetuses characterized by a large cystic hygroma in the nuchal region and a prominent and generalized edema, the structure and extension of the lymphatic system was studied. In all fetuses marked malformations of this system were found. Although the morphologic appearance seemed to vary greatly it is suggested that the disorder is essentially a generalized hypoplasia and partial agenesis of the lymphatic system, which ceases to extend peripherally at an early embryonic stage. A suggestion as to the mechanism of this growth inhibition is made.


Archives of Dermatological Research | 1988

The carcinogenic risks of modern tanning equipment: Is UV-A safer than UV-B?

H. van Weelden; F.R. De Gruijl; S. C. J. van der Putte; J. Toonstra; J.C. van der Leun

SummaryAn animal experiment is presented in which three groups of albino hairless mice (Skh-hr 1) were exposed to daily doses of either UV-B or UV-A to study carcinogenesis. The UV-A was filtered carefully so as to eliminate contaminating UV-B. The doses required for acute effects (erythema and edema) were also determined for the two radiation modalities. In order to study the relative carcinogenic risks of exposures to UV-A and to UV-B, for both modalities, the doses causing skin tumors were compared to the doses required for eliciting acute effects in the skin.In the experiment on carcinogenesis all animals developed tumors, the ones exposed to UV-A as well as the ones exposed to UV-B. A striking difference, however, was that the induction times of the first tumors showed a larger spread in the mice exposed to UV-A than in the UV-B groups. Also, the development of successive tumors in each individual mouse was more spread in time in the UV-A group. A second difference between the effects on the skin was that in the animals exposed to UV-B no skin reactions were seen until the tumors developed. However, in most UV-A exposed animals, a marked scratching, probably caused by severe itching, and hyperkeratosis preceded the development of the tumors.Histologically at least 60% of the larger tumors induced by UV-A appeared to be squamous cell carcinomas. This finding is very similar for UV-B induced tumors. The elastic fibers in the UV-A exposed animals were also examined and actinic elastosis was observed.Experience has proven that the doses for acute affects in man and mouse are at least proportional to human tanning doses. Comparison of the doses of UV-A and UV-B required for the induction of tumors and for acute reactions of the skin, therefore, leads to the conclusion that the carcinogenic risks of tanning by UV-A and of tanning by UV-B are in the same order of magnitude.


American Journal of Dermatopathology | 1995

Mammary Paget's disease confined to the areola and associated with multifocal Toker cell hyperplasia

S. C. J. van der Putte; J. Toonstra; A. Hennipman

A hitherto unreported variant of mammary Pagets disease (MPD) limited to the areola, leaving the nipple unaffected, has been analyzed by serial sectioning of the whole areola and nipple. This otherwise characteristic MPD proved to be confined to the epidermis. There was no underlying carcinoma. This MPD was associated with a multifocal presence of monomorphic but otherwise similar cells in small collections surrounding the ostia of areolar mammary glands in the clinically unaffected area. This condition was interpreted as hyperplasia of mammary gland-related cells also found in normal nipples (so-called Toker cells). The observations hint at a possible derivation of some cases of mammary and extramammary Pagets disease from such Toker cells.


Archives of Dermatological Research | 1990

UVA-induced tumours in pigmented hairless mice and the carcinogenic risks of tanning with UVA.

H. van Weelden; S. C. J. van der Putte; J. Toonstra; J.C. van der Leun

SummaryAn animal experiment is presented in which two groups of pigmented hairless mice were exposed daily to suberythemal doses of UVA to study tumourigenesis. The aim of the study was to estimate the carcinogenic risks of tanning by UVA. The pigmented hairless mice, Skh-hr2, were separated by selective breeding into two groups, the “browns” and the “blacks”. Both groups were exposed daily to UVA from fluorescent UVA lamps (Philips TL40W/09) purified by rigorously filtering out the shorter wavelengths. No acute actinic damage was observed after any exposure. However, in most UVA exposed animals, especially in the blacks, a marked scratching preceded the development of tumours. Hyperkeratosis was also observed. All animals developed tumours. Histopathologically at least 60% of the tumours were squamous cell carcinomas. Depositions of melanophages were observed, but no melanomas. It is beyond any doubt that UVA is carcinogenic in laboratory animals. The present state of knowledge justifies no preference for tanning with UVA over tanning with UVB.


American Journal of Dermatopathology | 1994

Apoeccrine glands in nevus sebaceus

S. C. J. van der Putte

Apoeccrine glands were found in 13 of 57 specimens of nevus sebaceus. The glands showed the basic structure of eccrine glands, but differed in that a part of the secretory duct was lined by characteristic apocrine epithelium. The apocrine alteration varied from slight apocrine changes in a few secretory cells to an almost complete alteration of the secretory epithelium in other glands. The association with changes in the excretory ducts of rare glands suggested a transformation of eccrine into apocrine glands. It was nevertheless considered as most likely that a majority of the apocrine glands in nevus sebaceus had developed in the «classic» way in association with pilosebaceus structures


Photochemistry and Photobiology | 1988

The dose-response relationship of tumorigenesis by ultraviolet radiation of 254 nm.

H. J. C. M. Sterenborg; S. C. J. van der Putte; J.C. van der Leun

Abstract— Groups of albino hairless mice, Skh‐hrl, were exposed daily to UVC radiation from low pressure Hg arcs (Philips TUV 40W). These lamps emit predominantly radiation of 254 nm. Three groups of animals were used in the experiments, each receiving a different daily dose.


Virchows Archiv B Cell Pathology Including Molecular Pathology | 1984

Malignant lymphoma of follicle centre cells with marked nuclear lobation

S. C. J. van der Putte; Henk Jan Schuurman; L. H. P. M. Rademakers; P. M. Kluin; J. A. M. van Unnik

SummaryFour cases of malignant B-cell lymphoma characterized by a conspicuous component of tumour cells with markedly lobtated nuclei are described. Two exhibited a follicular and two a diffuse growth pattern. The tumour cell population formed a continuous spectrum comprising both cells resembling normal follicle centre cells and multilobated lymphoma cells. Cytomorphological analysis of the multilobated cell group indicated a differentiation series from centroblast-like cells with moderately lobated nuclei to large and medium-sized cells with marked nuclear lobation which revealed features of centrocytes. In three cases (1, 3, and 4) the majority of these multilobated cells showed plasmacytoid differentiation in their cytoplasm in conjunction with the synthesis of monotypical cytoplasmic immunoglobulin. No plasmacytoid features were present in a fourth case (2). In only one case (4) monotypical surface immunoglobulin was detectable on the tumour cells.A close relationship between the multilobated tumour cells and follicle centre cells was further substantiated by the finding of a similar cell variant in the follicle centres of a control group of non-neoplastic lymph nodes. It included cells with plasmacytoid differentiation which synthesized polytypical immunoglobulin.We consider this type of B-cell lymphoma with a conspicuous component of cells with lobated nuclei as a variant of malignant lymphoma, centroblastic/centrocytic.


Archives of Dermatological Research | 1985

Actinic reticuloid simulating sézary syndrome

J. Toonstra; H. van Weelden; F. H. J. Gmelig Meyling; S. C. J. van der Putte; S. I. M. Schiere; H. Baart de la Faille

SummaryA report is given on two male patients who showed all the main characteristics of Sézary syndrome (SS). When phototested, however, they proved to be extremely photosensitive, which suggested a diagnosis of actinic reticuloid (AR). This was supported by the predominance in blood and skin specimens of lymphoid cells with a suppressor/cytotoxic phenotype, the absence of clonal cell proliferation and a benign clinical course. Differential diagnostic problems of SS and erythrodermic AR are discussed.

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Rein Willemze

Leiden University Medical Center

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C. J. L. M. Meijer

VU University Medical Center

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