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Overexpression of phosphorylated-STAT3 and phosphorylated-ERK protein in dermatofibrosarcoma protuberans.

The overexpression of phosphorylated signal transducer and activator of transcription-3 (p-STAT3) and phosphorylated extracellular signal-regulated kinase (p-ERK) have recently been shown to play an important role in the pathogenesis of various human tumors. However, the role of these two major signal transduction pathways in dermatofibrosarcoma protuberans (DFSP) remains unknown. This study was designed to investigate the significance of p-STAT3 and p-ERK expression in DFSP. The expressions of p-STAT3 and p-ERK were analyzed by immunohistochemical staining in formalin-fixed, paraffin-embedded tissue sections of human DFSP and dermatofibroma. Ten cases were positive for p-STAT3 expression in 14 cases of DFSP, however, only 5 cases were positive in 20 cases of dermatofibroma. Eleven out of 14 cases of DFSP expressed p-ERK, but only four cases were positive in 20 cases of dermatofibroma. The expressions of p-STAT3 and p-ERK were significantly higher than those in dermatofibroma (both p < 0.01). This study suggests that the overexpression of p-STAT3 and p-ERK may play a pivotal role in the oncogenesis of DFSP.

Adult↗

[Pulmonary metastasis of a dermatofibrosarcoma].

Progressive and recurrent dermatofibrosarcoma, described by Darier and Ferrand in 1924, is a fibrous skin tumour with essentially local malignancy. The authors report a case with pulmonary metastasis, a rare event as only 13 cases of visceral metastases have been reported in the literature. The clinical course of this case was favourable (follow-up of 5 years), in contrast with the usually pejorative nature of metastatic disease (death after several months to one year following the discovery of the first metastasis).

Fibrosarcoma↗

Surgical treatment of dermatofibrosarcoma protuberans. A retrospective study of 20 cases with review of literature.

The clinicopathological features and results of surgical treatment of 20 patients with dermatofibrosarcoma protuberans (DFSP) were reviewed. All patients have been observed until the present time or death. The primary treatment usually consisted of marginal, wide or radical excision. Re-excision because of recurrence was performed in six of the 20 patients who were treated primarily only by marginal excision. Following re-excision two patients have remained disease-free until the present, the other four of these six patients had a second recurrence. Three of these four patients with a second relapse were successfully treated by excision. Although six patients out of 20 had 13 recurrences at the site of primary therapy, no patient developed lymph node or distant metastases. To date, none of the remaining 14 patients has had recurrence, all having been treated by excision of from 1 to 5 cm, the mean follow-up time was 8.75 years. Based on our data, the high recurrence rate after marginal surgical treatment implies an initial radical resection.

Adult↗

Pigmented dermatofibrosarcoma protuberans (Bednár tumor). An autopsy case with systemic metastasis.

An autopsy case of pigmented dermatofibrosarcoma protuberans (Bednár tumor) with systemic metastasis is reported. No previous example of this tumor showing widespread metastasis has been reported in the literature. The patient, a 45-year-old man, developed a tumor on the right upper arm. The tumor recurred twice and metastasized to other parts of the skin, lungs and brain during the 8-year clinical course. The primary tumor contained melanin-laden tumor cells and showed a storiform growth pattern. Autopsy confirmed multiple metastatic lesions in the skin, lungs, brain, thyroid, pancreas, stomach, small intestine and thigh muscles. The recurrent and metastatic tumors lacked both melanin production and the storiform arrangement, and instead revealed "fibro-sarcomatous" change with a herring-bone or interlacing pattern of growth.

Adult↗

[An unusual case of dermatofibrosarcoma protuberans].

A case of Dermatofibrosarcoma Protuberans (DFSP) with unusual cystic features is described. It is difficult to evaluate the actual incidence of this feature on the basis of literature; on the other hand we observed it only once in a series of 27 patients studied from 1975-1989.

Fibrosarcoma↗

Bednar tumor (pigmented dermatofibrosarcoma protuberans). An analysis of six cases.

Six cases of Bednar tumor were analyzed clinicopathologically along with a review of 39 published cases. The findings were then compared with data on 44 cases of ordinary dermatofibrosarcoma protuberans (DFSP) obtained from our files. The clinical manifestations of the patients and the anatomic locations of the tumors were similar between the two categories, but the rate of recurrence was lower in cases of Bednar tumor. The histologic pattern of Bednar tumor was indistinguishable from ordinary DFSP except for scattered melanosome-containing cells. Ultrastructural and immunohistochemical examinations showed no evidence of neuroectodermal differentiation of dominant spindle-shaped cells in Bednar tumor, supporting a fibroblastic line of differentiation. The origin and pathogenesis of the melanosome-containing cells were considered. These cells failed to react with HMB-45, a melanoma-specific antibody, and the large majority of melanosomes present were mature or at Stage IV, plus a few immature ones at Stage II. These pigmented cells do not appear to be neoplastic, and cannot be used as proof to indicate that Bednar tumor is a neuroectodermal neoplasm.

Adolescent↗

[Metastatic Darier-Ferrand dermatofibrosarcoma. Review of the literature apropos of a case].

We report the case of a 56-year old male patient with pulmonary, abdominal and pelvic metastases from a dermatofibrosarcoma (DFS) which had developed 23 years previously in the right scapulo-humeral region and had recurred twice after the first excision, in 1983. Surgery was only performed once. The most remarkable feature of the disease was the progressive transformation, with each recurrence, of a typical DFS into a poorly differentiated and highly malignant tumour, about as active as a fibrosarcoma. A review of the literature yielded 31 cases of histologically proven metastatic DFS. Although the actual incidence of metastases is difficult to determine with accuracy, their frequency may be estimated at 3 p. 100 (most probably a maximum figure). The disease spreads mostly through the blood, but also sometimes through the blood and lymph. However, since lymphatic involvement is rare the usefulness of lymph node excision is extremely doubtful. Pulmonary lesions are the most frequent ones, but various other organs may be affected, although this seldom applies to the liver. Following a first excision, metastases occur within 6 years on average (range: 1 to 33 years). This mean delay is superior to the mean follow-up period for most of the important series without metastases. The histopathological picture is usually one of typical DFS but in some cases, including ours, it is much less typical and may even be frankly malignant. A few reports mention the presence of histiocytic infiltrates associated with the fibroblasts. The prognosis in patients with metastases is particularly poor: in most of the cases reported the patient died within the year following the discovery of metastatic lesions. The very high progressivity of the secondary lesions contrasts with the slow course of the primary tumour. None of the treatments tried (surgery, radiotherapy, chemotherapy) has resulted in a significant prolongation of life. No correlation can be established between the occurrence of metastases and the following parameters taken together: patient's age and sex, tim elapsed between the appearance of the tumour and the date of exicision, and histological features of the initial tumour. The development and number of recurrences seems to be the most significant predictive factor as regards the risk of metastasis. The noxious role of incomplete and/or repeated surgery creating vascular breaks, disrupting the defense barriers and encouraging malignancy in some cases has been mentioned by most authors; it emphasizes the value of the widest possible initial surgery.(ABSTRACT TRUNCATED AT 400 WORDS)

Fibrosarcoma↗

Dermatofibrosarcoma protuberans.

The authors describe a malignant tumor that is rarely encountered by the podiatric surgeon. Clinical presentation and treatment of choice are discussed along with a case report. The tendency for dermatofibrosarcoma protuberans to recur and to possibly metastasize makes accurate diagnosis, treatment, and careful follow-up essential.

Aged↗

[Clinical picture and pathology of dermatofibrosarcoma protuberans].

Dermatofibrosarcoma protuberans (D.p.) is a rare connective skin tumor (0.1%). On the basis of the literature and 13 own cases, we present data concerning age, sex, localisation, as well as clinical and histological findings. We report on pre-operative planning of treatment, surgical therapy (wide excision and closure by rotation flap), and clinical course. The follow-up indicates that D.p. is a neoplasia bearing a low rate of malignancy, which may change into a highly malignant tumor especially after treatment with radiation.

Adult↗

[Juvenile dermatofibrosarcoma protuberans].

Dermatofibrosarcoma protuberans is observed in younger or middle-aged patients after the transformation from the initial stage of a chronic fibrous plaque into a rapidly growing, sometimes painful or bleeding tumor. First manifestation in early childhood is considered in about 10 per cent of the reported patients. In the case that we observed the neoplasma was present at birth and increased to a multinodular tumor between three and four years of age. Repeated local recurrences in the scar were observed after the surgical removal. The clinical behavior of the tumor in childhood is comparable to those of adults. Because of its malignant potential extended early excision should be undertaken despite of the risk of widespread scarring.

Child↗

Effective radiotherapy in one case of dermatofibrosarcoma protuberans.

A case of dermatofibrosarcoma protuberans is presented where radiotherapy had been part of the management of multiple recurrent lesions. Over a course of 46 years, complete response occurred in 2 out of 3 lesions after medium-and high-dose radiation therapy and in 1 out of 5 lesions after interstitial therapy. Regression of the lesions took several months. In the literature, 5 additional cases of local control and 2 of partial control after high-dose radiotherapy are reported. When failure of radiotherapy was reported, the dose had been low and the observation time short in many cases. High-dose radiotherapy used with patience might be tried in selected cases.

Adult↗

Dermatofibrosarcoma protuberans: a case report and clinicopathologic review.

Dermatofibrosarcoma protuberans is a soft tissue, low-grade malignant tumor. Histologically, the tumor is a low-grade sarcoma with a constant storiform growth pattern. The tumor may possibly arise from histiocytes, a thesis supported by recent tissue culture and electron microscopic studies. Treatment consists of the wide local excision. Conservative excision often results in recurrences. Lymph node and other distant metastases, although rare, have been documented. Most often, the clinical course shows this tumor to be slow growing and often painless. Presented herein is a patient in whom this uncommon tumor developed.

Back↗

[Histogenesis of dermatofibrosarcoma protuberans].

In order to specify the histogenetic appurtenance of dermatofibrosarcoma protuberance, the ultrastructure of cells from three tumors was studied. The similarity between the ultrastructure of the tumor cells and normal fibroblasts suggests the fibroblastic origin of the tumor.

Fibroblasts↗

[Labyrinth nuclei as observed in dermatofibrosarcoma protuberans and fibroxanthoma (author's transl)].

In the electron microscope the nuclei of benign and malignant tumors as well as the nuclei of normal cells exhibit relatively various structural features. In this study the author reports on two mesenchymal tumors of the skin (one case of dermatofibrosarcoma protuberans and one of fibroxanthoma) with pecular nuclear polymorphism which can be visualized by electron microscopy only.

Adult↗

Dermatofibrosarcoma protruberans: analysis of eight cases in an African population.

Eight cases of dermatofibrosarcoma protruberans seen in the University College Hospital, Ibadan, Nigeria between 1960 and 1972 are reviewed. The condition is rare in this population and affects young adults of both sexes. All were treated by wide excision and skin grafting with no recurrence at follow-up. The apparently low incidence being reported may be due in part to the inconsistent histological pattern of the lesion. Clinicians are urged to be more aware of this condition when a cutaneous, nodular or multiobulated tumor is encountered.

Adolescent↗