Endocrinology, Diabetology and Medical Andrology Unit, Humanitas Clinical and Research Center - IRCCS -, Via Manzoni, 56, 20089, Rozzano, MI, Italy.
Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
J Endocrinol Invest. 2021 Mar;44(3):391-402. doi: 10.1007/s40618-020-01362-x. Epub 2020 Jul 20.
Testicular adrenal rest tumors (TARTs) are benign masses deemed to originate from pluripotent testicular steroidogenic cells that grow under chronic ACTH stimulation. These lesions, occasionally misdiagnosed as Leydig cell tumors (LCTs), are typically described in patients with congenital adrenal hyperplasia (CAH). X-linked adrenoleukodystrophy (X-ALD) is an inherited disorder of beta-oxidation with accumulation of very long chain fatty acids (VLCFAs) in various tissues, and a rare cause of primary adrenal insufficiency (PAI). TARTs have never been associated with X-ALD. CASE 1 DESCRIPTION: A 19-year old male, who had previously undergone bilateral enucleation of presumed LCTs, was referred to our unit. Follow-up scans showed persistent bilateral lesions compatible with TARTs. Biochemical exams revealed PAI but excluded CAH. A serum VLCFAs panel was consistent with X-ALD, with gene testing confirming the diagnosis. Histological revision of the previously resected testicular lesions was compatible with TARTs. Start of glucocorticoid replacement therapy was associated with a reduction of testicular masses. CASE 2 DESCRIPTION: A 26-year old X-ALD male was diagnosed with bilateral testicular lesions compatible with TARTs. These lesions increased after ACTH elevation following switch to modified-release hydrocortisone. Clinical and sonographic findings allowed for a "watchful-waiting" approach, avoiding unnecessary surgery.
These are the first cases reported of TARTs in patients with X-ALD-associated PAI. Testicular lesions in patients with an early onset of ACTH elevation, regardless of the cause, should always be thoughtfully investigated, as they may reveal themselves as TARTs. We suggest that all patients affected from chronic ACTH elevation of a young age of onset should undergo testicular ultrasound in order to evaluate the presence of these lesions. GRT in these patients might also help preserving fertility.
睾丸肾上腺残迹瘤(TART)被认为起源于多能性睾丸甾体生成细胞,这些细胞在慢性 ACTH 刺激下生长,是良性肿块。这些病变偶尔被误诊为莱迪希细胞瘤(LCT),在先天性肾上腺增生症(CAH)患者中较为常见。X 连锁肾上腺脑白质营养不良(X-ALD)是一种β氧化的遗传性疾病,各种组织中堆积极长链脂肪酸(VLCFA),是原发性肾上腺功能不全(PAI)的罕见原因。TART 从未与 X-ALD 相关。
病例 1 描述:一名 19 岁男性,此前曾行双侧疑似 LCT 切除术,被转至我院。随访扫描显示双侧病变持续存在,符合 TART。生化检查显示 PAI,但排除 CAH。血清 VLCFA 谱符合 X-ALD,基因检测证实了诊断。先前切除的睾丸病变的组织学复查与 TART 相符。开始糖皮质激素替代治疗后,睾丸肿块减少。
病例 2 描述:一名 26 岁 X-ALD 男性被诊断为双侧符合 TART 的睾丸病变。这些病变在改用控释氢化可的松后 ACTH 升高时增大。临床和超声检查结果允许采用“静观其变”的方法,避免不必要的手术。
这是首例报道的 X-ALD 相关 PAI 患者的 TART 病例。无论病因如何,对于早期 ACTH 升高的患者,睾丸病变都应仔细检查,因为它们可能表现为 TART。我们建议所有早期慢性 ACTH 升高的患者应进行睾丸超声检查,以评估这些病变的存在。这些患者的 GRT 也可能有助于保留生育能力。