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Biomedical subjects

F Eckert

Publications and source records attributed to F Eckert.

At least 55 records · Page 3Linked to original sources
PubMed1991

[Eccrine poroma. A clinico-pathologic and immunohistologic study with special reference to tumor cell differentiation].

In this study 15 eccrine poromas were analysed clinically, histologically and immunohistologically. They were all solitary lesions, showing a predilection for the head and neck. In none of the tumours was diagnosis possible on the basis of clinical examination. Histomorphologically, eccrine poromas were characterized by aggregations of neoplastic cells continuous with the epidermis. The neoplasms consisted of two cell types, poroid and cuticular. Poroid cells predominated, while cuticular cells were only found in small foci, sometimes showing tubular differentiation. Immunohistologically, most of the tumour cells showed a cytokeratin pattern (CK1, 5, 10, 11+, CK1-19+) favouring differentiation toward the abluminal cell of the dermal eccrine duct rather than toward the abluminal cell of the intraepidermal segment of the eccrine duct. Only a small proportion of cells revealed the immunohistological features of the abluminal cell of the intraepidermal duct (CK1+, CK1, 5, 10, 11+, CK1-19+). In addition, cuticular cells showed differentiation toward the luminal cell of the eccrine duct (CK19+, CK1, 5, 10, 11+, CK1-19+). Simple-type cytokeratins such as CK7 and CK18 were not expressed. In conclusion, our findings favour the hypothesis that ascribes the origin of eccrine poroma to a pluripotential stem cell of the transitional zone between the dermal and the intraepidermal segments of the eccrine duct.

Adenoma, Sweat Gland↗
PubMed1991

[Spinocellular cancers and myxoid atypical fibroxanthoma of an actinically damaged burn scar].

We report on a 66-year-old male patient suffering from several squamous cell carcinomas and a myxoid atypical fibroxanthoma of the skin. The tumours developed in burn scars that the patient had had for more than 50 years and that had in part undergone actinic elastosis. The role of burn scars in the development of different skin tumours is pointed out. In addition, we discuss the differential diagnosis of the rare myxoid variant of atypical fibroxanthoma.

Aged↗
PubMed1991

[Pseudo-Kaposi sarcoma in Prader-Labhart-Willi syndrome].

A 25-year-old male patient presenting with Prader-Labhart-Willi syndrome is reported. He had sought medical help because of lichenoid skin eruptions on his lower legs. Histologically the lesions turned out to be pseudo-Kaposi's sarcoma. The possible aetiopathologic relationship between the two primarily unassociated conditions is discussed.

Adult↗
PubMed1991

[Viscerocutaneous hemangiomatosis--the so-called blue-rubber-bleb nevus syndrome].

A case of so-called blue rubber bleb naevus syndrome in a 17-year-old girl is presented. Apart from multiple haemangiomas of the skin, further lesions were present in the small and large intestine, which were demonstrated by endoscopy. The features characterizing the syndrome as a separate entity within the group of angiomatous diseases are discussed.

Adolescent↗
PubMed1991

[Angiolymphoid hyperplasia with eosinophils. Case report and differentiation from Kimura disease].

We report a 40-year-old patient, who presented with a nodular tumor at the scalp. The histological diagnosis was angiolymphoid hyperplasia with eosinophils (ALHE). Immunohistochemical staining of the proliferating vessels was characteristic for endothelial cells. The perivascular inflammatory infiltrate mainly consisted of CD4-positive lymphocytes. Recently it has become clear that Kimura disease, which was thought to be a variant of ALHE, can be distinguished from ALHE by clinical, histological and immunohistochemical criteria and constitutes its own clinical identity. While ALHE is a localized proliferation of endothelial cells, Kimura disease is a proliferation of lymphoid cells characterized by invasive growth and possibly lymphadenopathy.

Adult↗
PubMed1991

[Pyostomatitis vegetans. A specific marker of Crohn disease and ulcerative colitis].

Pyostomatitis vegetans is a rare disease of the oral cavity with characteristic clinical and histopathological findings. Its importance lies in its high correlation with inflammatory diseases of the intestinal tract. The present case report and a review of the literature are taken as a basis to discuss the disease as an entity. Pyostomatitis vegetans is a specific marker for ulcerative colitis and Crohn's disease.

Adult↗
PubMed1990

Hodgkin's disease followed by lymphomatoid papulosis. Immunophenotypic evidence for a close relationship between lymphomatoid papulosis and Hodgkin's disease.

The clinical association of lymphomatoid papulosis and Hodgkin's disease and the striking morphologic similarity of atypical cells in lymphomatoid papulosis to Reed-Sternberg cells in Hodgkin's disease suggest that lymphomatoid papulosis and Hodgkin's disease are related. To test this possibility we studied the antigenic profile of Reed-Sternberg cells in the lymph nodes and of atypical cells in cutaneous lesions of lymphomatoid papulosis in two patients with Hodgkin's disease and lymphomatoid papulosis. In paraffin sections both cell types expressed CD30, CD45 T cell-restricted antigens, and occasionally CD15 antigens. They were negative for CD45 B cell-restricted antigens and for lysozyme. In cutaneous lymphomatoid papulosis lesions a similar immunologic profile of the atypical cells was found; that is, they were positive for CD30, CD2, CD3, and CD25 but negative for B cell and macrophage antigens. The similarity of the immunophenotype of Reed-Sternberg cells in lymph nodes affected by Hodgkin's disease and the immunophenotype of atypical cells of lymphomatoid papulosis lesions in the same patients suggests that the malignant cells in both conditions are derived from activated T cells and that they are closely related if not identical.

Adult↗
PubMed1990

Melanocytes of a melanocytic nevus in a lymph node from a patient with a primary cutaneous melanoma associated with a small congenital nevus.

Aggregates of melanocytes within the parenchyma of a supraomohyoid lymph node were found in a lymph node dissection from a 52-year-old woman who had a primary cutaneous melanoma that had arisen in association with a small congenital nevus. The melanocytes in the lymph node were interpreted to be those of a benign melanocytic nevus, and not those of malignant melanoma, based on similarities in morphologic features and immunohistochemical staining between the melanocytes in the node and those in the cutaneous congenital nevus.

Female↗
PubMed1990

Differentiation between lymphomas and pseudolymphomas of the skin by computerized DNA-image cytometry.

The histologic and immunohistologic differential diagnosis between pseudolymphomas (PL) and malignant lymphomas (ML) of the skin can be difficult. Since DNA cytometry has been found to be of both diagnostic and prognostic value in various neoplasms, its ability to discriminate between ML and PL in Feulgen-stained imprints of 17 PL and 49 ML skin biopsies was examined by high-resolution image analysis. The reliability of the following algorithms of DNA distribution was evaluated: 1) 2cDI (2c-deviation index), which reflects the variation of the nuclear DNA values around the diploid DNA peak; 2) percentage of cells having a DNA value greater than or equal to 5c (5cER; 5c-exceeding rate); 3) percentage of cells presenting with a DNA value greater than or equal to 4c (4cER). A 2cDI of 0.1 was found to be the most reliable marker for the differentiation between PL and ML. On the basis of this feature, 16 of 17 cases of PL and 46 of 49 cases of ML were correctly classified. The sensitivity, specificity, and efficiency of this feature were 94%. A 5cER greater than or equal to 1% had a specificity of 100%, but the sensitivity was only 43%. For the 4cER, a sensitivity of 61% and a specificity of 94% were found. In conclusion, the calculation of the 2cDI and the 5cER based on high-resolution image analysis provided additional helpful diagnostic features, and therefore should be included as a diagnostic tool. If the 5cER is at least 1%, the diagnosis of a ML can be confirmed with a specificity of 100%.

Cytophotometry↗
PubMed1990

[Multiple eccrine spiradenomas in a linear nevoid pattern].

A 16-year-old boy presenting with multiple slightly painful, bluish red papules and plaques on the left thorax is reported. The skin lesions were arranged in a linear and arched pattern following the lines of Blaschko. Clinical examination led to the suspicion of multiple leiomyomas, syringomas or glomus tumours. Histological examination revealed that the lesions were typical benign eccrine spiradenomas.

Adenoma, Sweat Gland↗
PubMed1990

[To be or not to be].

It's all about life in an intensive care unit. Of course, there is an organic aspect of life, the maintenance of which relies on a knowledge. Playing with a human being, life relies also on a psychological aspect and the temptation is great to answer the problematical by knowledge as well. But such an attitude would be most inoperative. It could only serve the therapeutist in economizing his own psychological engagement in the relation with the patient. In the confrontation between patient and therapeutist, isn't it rather a question of existential work between two protagonists during which the patient would be fighting for the maintenance or the restitution of his own person, while the therapeutist tries to maintain his.

Critical Care↗
PubMed1990

Congenital multiple plaquelike glomus tumors.

We encountered two patients with congenital multiple plaquelike glomus tumors. These lesions were present at birth and enlarged with body growth, attaining a diameter of up to 13 cm. The diagnosis was confirmed by histologic and electron-microscopic examination, which revealed the typical changes of glomus tumors. Immunocytochemistry findings demonstrated the tumor cells to be vimentin- and alpha-smooth muscle-actin-positive and desmin-negative. On ultrastructural examination, typical dense bodies and attachment plaques were easily found within the tumor cells. Glomus cells were coated by a thick basal lamina.

Child↗
PubMed1990

[The atypical fibroxanthoma].

A 84-year-old female patient suffering from atypical fibroxanthoma is presented. A diagnosis of malignant melanoma or a cutaneous metastasis from an unknown primary tumor was suspected. The final diagnosis was established by immunohistological studies showing a strongly positive reaction to vimentin and a negative reaction to S-100 protein and cytokeratin.

Aged↗
PubMed1990

[Pseudolymphoma following tattooing].

A single pseudolymphoma in the area of a tattoo is reported. Histological examination revealed an infiltrate composed of lymphocytes and histiocytes, and also confluent epithelioid cell aggregates without germinal centres. Immunohistologically, mainly T-lymphocytes and dendritic cells were demonstrable.

Adult↗
PubMed1990

[Encapsulated neuroma of the skin. A clinical, histologic and immunohistologic study].

Encapsulated neuroma of the skin is a little known, though not especially rare, benign tumour of the peripheral nerve system. It is often wrongly diagnosed on the basis of both clinical and histological investigation. We have subjected 24 encapsulated neuromas to clinical, histological, and immunohistological study. Clinically, they presented as solitary, skin-coloured small nodules, usually located on the face in middle-aged adults. Histologically, encapsulated neuromas are well-circumscribed dermal tumours. They are composed of interlacing fascicles of Schwann cells (S-100 protein +) and numerous tiny axons (S-100 protein +, neurofilament +). Most reveal at least partial encapsulation with perineurial differentiation (EMA +, vimentin +). Encapsulated neuromas can be differentiated from other tumours of the peripheral nerve system and from leiomyoma by their distinctive histological and immunohistological features.

Adult↗