Department of Pathology, Johns Hopkins Hospital, Baltimore, MD 21231, USA.
Am J Surg Pathol. 2013 Aug;37(8):1208-14. doi: 10.1097/PAS.0b013e318286c129.
Benign intratesticular spindle cell lesions are rare. Herein, we report the morphology, immunohistochemical characteristics, and prognosis of 16 cases of testicular fibrothecoma. The mean age at diagnosis was 44 years (16 to 69 y). Of 15 patients with information, 14 presented with a palpable testicular mass and 1 with heaviness in the scrotum. Medical histories included bilateral orchidopexy as a child (n=1) and testicular atrophy receiving testosterone replacement (n=1). The average size was 1.8 cm (median 2 cm; range, 0.5 to 7.6 cm). All cases were intratesticular, although 13 were abutting the tunica albuginea with others centered on the rete testis (n=2), or were indeterminate on biopsy (n=1). Eleven cases were relatively well circumscribed, although not encapsulated, with 1 being infiltrative and 4 not evaluable. Four tumors showed entrapment of seminiferous tubules. Half of the fibrothecomas showed a mixed storiform pattern and short fascicles, with 6 storiform only and 2 short fascicles only. One half of the tumors were very hypercellular. Cases were equally split between having plumper ovoid as opposed to spindled pointed nuclei, with all cases lacking prominent nucleoli. Eleven cases had 0 to 2 mitoses per 10 HPF, 3 had 4 to 5 mitoses per 10 HPF, and 2 had 9 to 10 mitoses per 10 HPF. Collagen deposition either in bands or investing single cells ranged from none to extensive, with 10/16 cases having at least a moderate amount. Immunohistochemical positivity was as follows: inhibin (11/13, patchy to diffuse); calretinin (5/9); Melan-A (4/4); pan keratin (5/8); BCL2 (3/4); CD34 (3/8); S100 (4/8); muscle-specific actin (4/4); and desmin (5/8). Patients were followed up for a mean of 71.8 months (range, 3 to 144 mo). All were well with no evidence of disease. Of the 2 men with 9 to 10 mitoses per 10 HPF, 1 died of other causes 5 years and 8 months later, and the other had no evidence of disease at 4 years and 10 months after surgery. In summary, testicular fibrothecomas are rare with somewhat variable histology and can have worrisome histologic features such as minimal invasion into surrounding testis, high cellularity, and increased mitotic rate. Their immunoprofile is variable and typically not diagnostic. Despite some worrisome histologic features, they appear uniformly benign in their behavior.
良性睾丸间质细胞病变较为罕见。本文报道了 16 例睾丸纤维卵泡膜细胞瘤的形态学、免疫组化特征和预后。诊断时的平均年龄为 44 岁(16 至 69 岁)。15 例患者中有 14 例表现为可触及的睾丸肿块,1 例表现为阴囊沉重。病史包括儿童期双侧隐睾(1 例)和接受睾酮替代治疗的睾丸萎缩(1 例)。平均大小为 1.8cm(中位数 2cm;范围,0.5 至 7.6cm)。所有病例均位于睾丸内,尽管 13 例紧邻白膜,另 13 例位于睾丸网中心(2 例)或活检不确定(1 例)。11 例肿瘤界限相对清楚,虽然无包膜,但 1 例浸润性,4 例不可评估。4 例肿瘤可见曲细精管被挤压。一半的纤维卵泡膜细胞瘤表现为混合性席纹状模式和短束状,6 例仅为席纹状,2 例仅为短束状。一半的肿瘤细胞非常丰富。肿瘤细胞核呈卵圆形或梭形,核仁不明显,半数细胞核呈卵圆形,另一半细胞核呈梭形。11 例每 10HPF 有 0 至 2 个有丝分裂,3 例每 10HPF 有 4 至 5 个有丝分裂,2 例每 10HPF 有 9 至 10 个有丝分裂。胶原沉积无论是成带还是围绕单个细胞,范围从无到广泛,16 例中有 10 例有中等量的沉积。免疫组化阳性结果如下:抑制素(13/13,弥漫或局灶性);钙视网膜蛋白(5/9);黑素-A(4/4);广谱细胞角蛋白(5/8);BCL2(3/4);CD34(3/8);S100(4/8);肌特异性肌动蛋白(4/4);结蛋白(5/8)。患者平均随访 71.8 个月(3 至 144 个月)。所有患者均预后良好,无疾病证据。2 例有丝分裂率为 9 至 10/10HPF 的患者中,1 例在 5 年后 8 个月因其他原因死亡,另 1 例在手术后 4 年 10 个月时无疾病证据。总之,睾丸纤维卵泡膜细胞瘤较为罕见,组织学形态有些变异,可能具有一些令人担忧的组织学特征,如微小浸润周围睾丸、高细胞性和有丝分裂率增加。其免疫组化表现多样,通常无诊断意义。尽管存在一些令人担忧的组织学特征,但它们的行为表现始终良性。