Lodding P, Kindblom L G, Angervall L
Department of Pathology II, University of Gothenburg, Sahlgren Hospital, Sweden.
Virchows Arch A Pathol Anat Histopathol. 1990;417(5):377-88. doi: 10.1007/BF01606026.
Metastases of cutaneous malignant melanoma (MM) of ordinary type can resemble various types of soft tissue sarcoma light microscopically to a degree which has not been previously recognized. Twenty-one cases are described, in which the tumours were originally diagnosed as a soft tissue sarcoma. Seven tumours were predominantly of blue and spindle-cell, fascicular type, resembling malignant peripheral nerve sheath tumour and at times monophasic synovial sarcoma. Ten tumours which were of fascicular and predominantly storiform type, and included uni- and multi-nuleated pleomorphic cells resembled malignant fibrous histiocytoma. Due to the presence of multivacuolated lipoblast-like tumour cells, 2 of these 10 tumours resembled pleomorphic liposarcoma. One had a predominantly myxoid and hypocellular appearance and 5 additional tumours included such areas. The diagnoses were revised after ultrastructural examination with the demonstration of melanosomes in 13 of 16 studied cases and the immunohistochemical demonstration of positivity using anti-S-100 protein antibodies and the anti-melanoma antibody NKI/C3 in all cases. The anti-melanoma antibody HMB 45 gave a positivity in 9 of 21 cases. Light microscopically, sparse amounts of melanin were noted in 7 tumours using the Whartin-Starry technique. Eleven tumours occurred at sites close to major lymph node groups and in 9 of these cases, lymphoid tissue was associated with the tumours, suggesting that they represented lymph node metastases. Following a review of the patients' clinical histories and renewed clinical examination, primary cutaneous MM was demonstrated in 10 of 21 patients and in 1 case an MM in regression was detected. The origin of the 10 tumours without a detected primary is discussed, including the possibility of an overlooked primary, spontaneous regression of a primary and a de novo origin from lymph nodes and soft tissues.
普通型皮肤恶性黑色素瘤(MM)的转移灶在光镜下可在一定程度上类似于各种类型的软组织肉瘤,这一程度是此前未被认识到的。本文描述了21例病例,这些肿瘤最初被诊断为软组织肉瘤。7例肿瘤主要为蓝色和梭形细胞、束状型,类似于恶性外周神经鞘瘤,有时也类似于单相滑膜肉瘤。10例肿瘤为束状且主要为席纹状型,包括单核和多核的多形性细胞,类似于恶性纤维组织细胞瘤。由于存在多空泡脂母细胞样肿瘤细胞,这10例肿瘤中有2例类似于多形性脂肪肉瘤。1例主要表现为黏液样和细胞稀少,另外5例肿瘤也包含此类区域。在16例研究病例中有13例经超微结构检查发现黑素小体,且所有病例经免疫组化显示使用抗S-100蛋白抗体和抗黑色素瘤抗体NKI/C3呈阳性后,诊断得以修正。抗黑色素瘤抗体HMB 45在21例病例中有9例呈阳性。光镜下,使用沃辛-斯塔里技术在7例肿瘤中发现了少量黑色素。11例肿瘤发生在靠近主要淋巴结群的部位,其中9例病例中,肿瘤与淋巴组织相关,提示它们代表淋巴结转移。在回顾患者临床病史并重新进行临床检查后,21例患者中有10例证实存在原发性皮肤MM,1例检测到处于消退期的MM。讨论了10例未检测到原发灶的肿瘤的起源,包括可能存在被忽视的原发灶、原发灶的自发消退以及淋巴结和软组织的新发起源。