Yamada Sohsuke, Nawata Aya, Yoshioka Manabu, Hiraki Tsubasa, Higashi Michiyo, Hatanaka Kazuhito, Tanimoto Akihide
Department of Pathology, Field of Oncology, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, Japan.
Department of Pathology and Cell Biology, School of Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.
BMC Res Notes. 2016 Jul 26;9:366. doi: 10.1186/s13104-016-2174-4.
Malignant melanoma (MM) tends to be spontaneously regressed, however, complete regression of primary cutaneous MM is an extremely rare phenomenon. Our aim is to be aware that pathologists and/or dermatologists can readily misinterpret it as the other benign or malignant lesions.
A gradually growing and verrucous hypopigmented macule had been noticed in the right sole of a 65-year-old Japanese male since 2 years before, and it turned to be a solitary bluish to black patch with surrounding depigmentation and was recently decreased in size. In parallel, the patient had a rapidly growing black-pigmented mass lesion at the right inguen. The cutaneous specimen from the sole showed an aggregation of many melanophages predominantly in the middle to deep layer of dermis, associated with surrounding fibrosis, reactive vascular proliferation and CD8-positive T-lymphocytic infiltrate, covered by attenuated epidermis with absence of rete ridge. However, no remnant MM cells were completely seen in the step-serial sections. We first interpreted it as blue nevus. By contrast, the inguinal mass revealed a diffuse proliferation of highly atypical mono- to multi-nucleated large cells having abundant eosinophilic cytoplasm in the enlarged lymph node tissue. Immunohistochemical findings demonstrated that these atypical cells were specifically positive for HMB45 and Melan A. Therefore, we finally made a diagnosis of complete regression of primary cutaneous MM associated with distant lymph node metastasis of MM.
Careful, not only general/cutaneous but histopathological, examinations should be necessary and adjunctive aids for reaching the correct diagnosis of complete regression of cutaneous MM.
恶性黑色素瘤(MM)往往会自发消退,然而,原发性皮肤MM的完全消退是一种极为罕见的现象。我们旨在提醒病理学家和/或皮肤科医生,这种情况很容易被误诊为其他良性或恶性病变。
一名65岁日本男性的右脚底自2年前起出现一个逐渐增大的疣状色素减退斑,后来变成一个孤立的蓝黑色斑块,周围有色素脱失,且近期尺寸减小。与此同时,患者右腹股沟出现一个迅速增大的黑色色素沉着肿块病变。取自脚底的皮肤标本显示,真皮中至深层有大量噬黑素细胞聚集,伴有周围纤维化、反应性血管增生和CD8阳性T淋巴细胞浸润,表面覆盖的表皮变薄,无 rete 嵴。然而,在连续切片中未完全见到残留的MM细胞。我们最初将其诊断为蓝痣。相比之下,腹股沟肿块在肿大的淋巴结组织中显示出高度非典型的单核至多核大细胞弥漫性增生,这些细胞具有丰富的嗜酸性细胞质。免疫组化结果表明,这些非典型细胞对HMB45和Melan A呈特异性阳性。因此,我们最终诊断为原发性皮肤MM完全消退并伴有MM远处淋巴结转移。
要正确诊断皮肤MM的完全消退,不仅需要仔细进行一般/皮肤检查,还需要进行组织病理学检查及辅助检查。