Rocamora A, Badía N, Vives R, Carrillo R, Ulloa J, Ledo A
J Am Acad Dermatol. 1987 Jun;16(6):1163-8. doi: 10.1016/s0190-9622(87)70151-0.
Three cases of primary cutaneous neuroendocrine carcinoma involving the face are reported. In the first patient the tumor developed in the scar of a previously excised basal cell carcinoma of the nose, recurred locally, and metastasized to a regional lymph node 2 1/2 years after initial treatment. In the second and third patients the tumors were located on the forehead and were removed with a wide excision. In the second patient the tumor metastasized to regional lymph nodes 1 month after treatment. Light microscopic examination in all patients showed an undifferentiated, small cell, dermal tumor with prominent epidermotropism, forming Pautrier-like microabscesses. Immunohistochemical staining for neuron-specific enolase was positive, and ultrastructural examination revealed numerous cytoplasmic neurosecretory granules and paranuclear aggregates of intermediate-sized filaments. The literature concerning epidermal involvement by primary neuroendocrine carcinoma of the skin is reviewed; the relation with basal cell carcinoma and treatment are discussed.
报告了3例累及面部的原发性皮肤神经内分泌癌。首例患者的肿瘤发生于先前切除的鼻基底细胞癌瘢痕处,局部复发,并在初始治疗2年半后转移至区域淋巴结。第二例和第三例患者的肿瘤位于前额,行广泛切除。第二例患者在治疗1个月后肿瘤转移至区域淋巴结。所有患者的光镜检查显示为未分化的小细胞真皮肿瘤,具有显著的亲表皮性,形成Pautrier样微脓肿。神经元特异性烯醇化酶免疫组化染色呈阳性,超微结构检查显示有大量细胞质神经分泌颗粒和中等大小细丝的核旁聚集物。复习了有关原发性皮肤神经内分泌癌累及表皮的文献;讨论了其与基底细胞癌的关系及治疗。