[Clinicopathologic characterization of malignant mixed tumor of the skin accompanied by eccrine porocarcinoma].

Objective: To investigate the clinicopathologic features, immunophenotype, pathological diagnosis and treatment of malignant mixed tumor (MMT). Methods: Clinical and pathological features including immunohistochemical phenotypes were analyzed in a case of MMT accompanied with eccrine porocarcinoma (EP) involving both hands, diagnosed definitely in January 2018 along with review of relevant literature. Results: A 64-year-old man presented with multiple rash on both hands for 4 years. Three lesions of 0.5 to 2.2 cm were removed for pathological evaluation. The pathological changes on little finger of left and right hands were MMT with EP, whereas that removed from the right ring finger was EP. MMT showed infiltrative growth with vascular wall invasion and consisted of epithelial (glandular or tube differentiation) and mesenchymal components (mucinous and/or cartilage stroma). The endothelial cells showed moderate to severe cytological atypia, nuclear pleomorphism and increased mitotic activity. The glandular component had histological characteristics of syringocarcinoma with moderately atypical chondrocytes but without myoepithelium. EP was composed of basal cells with visible vacuoles in cytoplasm and the presence of tubular and squamous differentiation, along with obvious atypia. Immunohistochemically cavosurface epithelium of glandular differentiation of MMT showed positivity for CK7, EMA and CD117. Myoepithelium showed S-100, CK5/6 and p63 positivity and stromal cells were positive for S-100. Differential diagnoses included metaplastic carcinoma, malignant myoepithelioma and atypical mixed tumor of skin. Conclusions: MMT with EP is extremely rare.The diagnosis of MMT depends on the morphologic features. Immunohistochemical staining is helpful for differential diagnosis. Surgical excision with safety margins is the treatment of choice. Complementary radiotherapy and/or chemotherapy is still controversial. The clinical course of MMT is deemed unpredictable and long-term follow-up is necessary.

Cytopathology in the diagnostic appraisal of uncommon malignant neoplastic lesions.

Cytology and fine needle aspiration (FNA) cytology are accepted means of diagnosing and typing of common forms of malignant tumors. However, their usefulness for diagnosing less common neoplasms is not clearly established and this study was designed to examine this. We report four unusual cases of patients with malignant neoplasms in which cytology and fine needle aspiration cytology or aspiration biopsy (FNAC, FNAB) contributed significantly in establishing the diagnosis. These cases facilitate the diagnostic capabilities of cytology over a wide spectrum of neoplasms including rare lymphoproliferative disorders and carcinomas.

[Eccrine porocarcinoma of the scalp]. / Saçli derinin ekrin porokarsinomu.

OBJECTIVE: Eccrine porocarcinoma is a rare malignant tumor of eccrine sweat glands. It may arise de novo, but it usually develops in pre-existing eccrine poroma. Here we report a case of eccrine porocarcinoma in the grafted area on the scalp of a male patient who had recurrent basal cell carcinoma of the scalp, with clinical, histopathological and, immunohistochemical features. CASE: We report a case of eccrine porocarcinoma in 78-year-old male patient who had recurrent basal cell carcinoma of the scalp. The tumor was polypoid, granular and heterogenous colored. Microscopic examination revealed a tumor composed of basaloid-poroid neoplastic cells in the dermis which showed solid and cystic areas. Focal clear cell change, and atypical and frequent mitoses were also observed. Neoplastic cells were diffusely positive with pankeratin. There was focal positivity with EMA and CEA. CONCLUSION: Eccrine porocarcinoma is a rare tumor. There are no large series that evaluate the diagnosis, monitoring and treatment of these tumors. In addition, this entity has to be kept in mind in the differential diagnosis of epidermal and skin appendix tumors.