Yu-Lin Gu, Wei-Jun Gu, Jing-Tao Dou, Zhao-Hui Lv, Jie Li, Sai-Chun Zhang, Guo-Qing Yang, Qing-Hua Guo,Jian-Ming Ba, Li Zang, Nan Jin, Jin Du, Yu Pei, Yi-Ming Mu

Abstract

Key words: Bilateral adrenocortical adenomas; Adrenocorticotropic hormone-independent Cushing’s syndrome; Adrenal venous sampling; Case report

INTRODUCTION

Inappropriate exposure to excessive concentrations of free glucocorticoids results in Cushing’s syndrome (CS)[1], with the clinical features of centripetal obesity, moon face,hirsutism, plethora, and striae, among others. The excess of glucocorticoid comes from endogenous or exogenous sources[2]. Endogenous causes of CS are rare. The incidence rates of CS are estimated to be 2 to 3 cases per million people per year in Europe and 10-15 cases per million people per year in America[3]. Some studies have revealed that subclinical hypercortisolism is significantly more possible in patients with bilateral incidentalomas[4]. Endogenous CS can be divided into adrenocorticotropic hormone (ACTH)-independent and -dependent forms. ACTHindependent CS is mostly due to unilateral tumors, with bilateral tumors rarely reported. Its main causes include ACTH-independent macronodular adrenal hyperplasia (AIMAH), primary pigmented nodular adrenocortical disease (PPNAD),and bilateral adrenocortical adenomas (BAAs) or carcinomas[5,6]. BAAs causing ACTH-independent CS are rare; up to now, fewer than 40 BAA cases have been reported. The accurate diagnosis and evaluation of BAAs are critical for determining optimal treatment options. Herein, we report a Chinese patient with BAAs, who was diagnosed with ACTH-independent CS by adrenal vein sampling (AVS) and computed tomography (CT).

CASE PRESENTATION

Chief complaints

A 31-year-old woman, who complained of gaining body weight, red face, moon face,bruising, and menstrual irregularity for two years, presented to our outpatient department.

History of present illness

The patient’s symptoms started two years ago with weight gain, red face, moon face,bruising, and menstrual irregularity.

History of past illness

She was diagnosed with hypertension a month ago and was medicated with nifedipine delayed-release tablets (II) 40 mg twice a day. Her family history was negative.

Physical examination

Physical examination revealed centripetal obesity, moon face, buffalo hump, thin skin,hirsutism, acne, striae on her abdomen, arms, and legs, and edema of both lower extremities. The height of this patient was 159 cm, and her body weight was 73.5 kg.Her blood pressure was 130/100 mmHg, with a pulse of 84 beats per minute.

Laboratory examinations

Her blood counts were within the normal limits, and she had no serum electrolytes disorders. The biochemical data showed dyslipidemia. The oral glucose tolerance test showed impaired glucose tolerance (IGT) and obviously increased insulin and Cpeptide levels. The endocrinological data showed elevated cortisol (761.0 nmol/L)and 24-h urine free cortisol (UFC) (1650.7 nmol/L) and the absence of a circadian rhythm and a non-suppression response to dexamethasone (dexamethasone 0.5 mg every 6 h for 2 d and 2 mg every 6 h for 2 d) administration (Table 1).

Imaging examinations

Abdominal CT showed bilateral adrenal adenomas with atrophic adrenal glands(right: 3.1 cm × 2.0 cm × 1.9 cm; left: 2.2 cm × 1.9 cm × 2.1 cm), which were enhanced homogeneously with contrast material (Figure 1). A magnetic resonance imaging(MRI) scan of the pituitary gland demonstrated normal findings.

Further diagnostic work-up

The patient was further evaluated with 1-deamino-8-D-arginine-vasopressin(DDVAP). The peripheral DDVAP stimulation test showed a baseline ACTH level of 6.9 pmol/L, and ACTH reached a peak level (7.26 pmol/L) at 90 min after stimulation, which was 1.05 times as high as the baseline level (Table 2). Then, we performed bilateral AVS to examine if the two adenomas were cortisol-secreting.Bilateral AVS results were as follows: the left-side adrenal vein (LAV)-to-peripheral vein (PV) cortisol gradient was 16.00; the right-side AV (RAV)-to-PV gradient was 8.29; and the ratio of the LAV cortisol-to-left side aldosterone (ALD) gradient to the RAV cortisol-to-right side ALD gradient was 1.23 (Table 3).

MULTIDISCIPLINARY EXPERT CONSULTATION

Jing-Tao Dou, MD, PhD, Professor and Chief, Department of Endocrinology,Chinese PLA General Hospital

It is important to know which side is functioning, which is hard to determine by imaging. We can do bilateral AVS to examine if the two adenomas are cortisolsecreting.

Ju-Ming Lu, MD, PhD, Professor and Chief, Department of Endocrinology, Chinese PLA General Hospital

BAAs often: (A) occur in mid-aged females; (B) have varying clinical symptoms; (C)are a kind of ACTH-independent CS, with hypercortisolism, absence of serum cortisol diurnal rhythm, and elevated UFC, though ACTH is in the normal range; (D) are 2.0-3.5 cm in diameter on CT; and (F) have normal finding in MRI of the pituitary. We should determine the source of ACTH, and testing the rhythm of ACTH-F is important.

Yong Song, MD, PhD, Assistant Professor, Department of Urology, Chinese PLA General Hospital

The patient should undergo surgical treatment twice separately after obtaining the result of bilateral AVS.

Table 1 Endocrinological study at different periods of bilateral adrenocortical adenomas

FINAL DIAGNOSIS

The final diagnosis was ACTH-independent CS and BAAs.

TREATMENT

A left adenomectomy by retroperitoneoscopy was performed on June 21, 2016.Irregular gray yellow tissue that measured 3.5 cm × 2.5 cm × 1 cm was observed on the left side. The cut surface was solid and golden yellow in color. Histologically, a single well-encapsulated adrenocortical tumor was observed in the adrenal gland. The Weiss score was 1. The immunohistochemistry results revealed MelanA(+), CgA(-),Syn(+), Ki-67(+2%), Inhibin-a(+), CK(-), and S-100(spotty+) (Figure 2A, 2B and Figure 3). Resection of the right-side adrenal mass was performed 3 mo later. The biopsy revealed nodular tissue on the right side measuring 2 cm × 1.8 cm × 1.5 cm. The cut surface was golden yellow in color. The Weiss score was 1. The immunohistochemistry results revealed MelanA(+), CgA(-), Syn(+), Ki-67(+2%), Inhibin-a(+),CK(-), S-100(spotty +) (Figure 2C, 2D and Figure 4).

OUTCOME AND FOLLOW-UP

Evaluations of ACTH and cortisol showed a significant decrease after the surgery. All of her symptoms were alleviated, and she had normal blood pressure and no edema in either of her lower extremities. She was administered with prednisone 20 mg once a day for half a month, which was then tapered to 15 mg once a day for a month and 5 mg twice a day, and finally 2.5 mg twice a day. The last follow-up was on June 5,2017, at which point all of her symptoms and signs have been alleviated (Figure 5).

DISCUSSION

Our case was confirmed as ACTH independency based on: (1) Very low plasma ACTH with increased serum cortisol level; (2) Unresponsiveness to a high-dose dexamethasone suppression test; (3) Unresponsiveness to a DDVAP stimulation test;and (4) MRI scan of the pituitary gland demonstrated normal findings; however, CT showed bilateral adrenal adenomas with atrophic adrenal glands. According to the tests above, ACTH-independent CS was diagnosed. Cases of ACTH-independent CS associated with adrenocortical adenoma are secondary to unilateral adrenocortical adenomas in approximately 90% of cases[7]. In contrast, bilateral cortisol-secreting tumors are a rare cause of CS[8].

Figure 1 Abdominal computed tomography images. Abdominal computed tomography images show bilateral adrenal adenomas with atrophic adrenal glands. Arrows indicate tumors with a low density (right, 3.1 cm × 2.0 cm ×1.9 cm; left, 2.2 cm × 1.9 cm × 2.1 cm). Tumors are homogeneously enhanced in the presence of contrast material.

As we know, the possibilities of bilateral adrenal space-occupying lesion are mainly: (1) BAAs; (2) Carcinomas; (3) PPNAD; and (4) AIMAH. Markedly enlarged bilateral hyperplastic adrenal glands with multiple macronodules up to 5 cm in diameter are a characteristic histopathological feature of AIMAH[1]. This disorder may be associated with other receptors besides ACTH, which are expressed in the adrenal cortex ectopically, such as gastric inhibitory polypeptide, luteinizing hormone/human chorionic gonadotropin and others[9,10]. PPNAD is another bilateral adrenal hyperplastic disease; CT scan shows bilateral small discrete nodules between 2 and 5 mm in size without overall enlargement of the glands. The possible mechanism may be a novel mutation in the type lα regulatory subunit of the protein kinase A(PRKAR1A) gene: p.E17X (c.49G＞T), which confirms that the diagnosis of PPNAD could be one component of Carney complex[11]. While carcinoma seems much more aggressive, with a heavier and larger mass, it is always complicated with severe hypertension, masculinization, hypokalemia, or alkalosis. On CT scan, the tumor is generally bigger than 5 cm in diameter, with heterogeneous enhancement with contrast agent[12]. BAAs were first reported by CHAPELL in 1963[13]. To the best of our knowledge, fewer than 40 BAAs cases have been reported. BAAs are the most significant feature of this case.

The mechanism of BAAs is unclear. Some studies have revealed that steroidogenic enzymes, such as P450scc, 3β-HSD, P450c21, P450c17, and P450c11, are intensely expressed in the compact cells of the adenoma, while their expression profiles are negative in the adjacent non-neoplastic cortex. At the same time, the histological features may differ between two adenomas[14,15]. It is difficult to distinguish between functioning or nonfunctioning adrenal cortical masses by the imaging characteristics on CT scanning[1]. AVS is a helpful method to distinguish between these conditions.The compound 6 beta-(131I)-iodomethyl-19-norcholesterol (NP-59) is another possible means for evaluating the function of an adenoma; however, NP-59 scintigraphy is never a common imaging modality in China. AVS provides important information concerning the laterality of excessive ALD, but it also has advantages compared with adrenal scintigraphy and CT in the diagnosis of CS and BAAs[16,17]. However, only a few cases have been reported with the use of AVS in the diagnosis of BAAs before surgery. According to the Mayo Clinic[16], AV-to-PV cortisol gradient greater than 6.5 is more likely to be a cortisol-secreting adenoma. In our case, the gradient of LAV-to-PV cortisol was 16, and the RAV-to-PV cortisol gradient was 8.2. The “ALDcorrected” high-side to low-side AV cortisol gradient was 2.3 or greater, which is consistent with autonomous cortisol secretion from predominantly one adrenal gland;a gradient of 2.0 or less indicates bilateral cortisol hypersecretion. The ratio of L/R of our patient was 1.23, less than 2.0. All of these pieces of evidence indicated that the hypersecretion of cortisol might originate from both adrenal glands. The first case of BAAs in China was reported in the medical literature by our team[18]. However, the AVS technique was not available at that time; therefore, we could not determine which side was functioning before the surgery.

Extirpation of the functioning adenoma is the optimal choice for bilateral CS adenomas[19]. AVS is a useful accessory examination before surgery to design a surgical plan that makes much more sense. Some authors believe that if AVS is unavailable, the larger of the two adenomas should be removed first, and then further management should be determined according to the postoperative hormone tests.However, at least 5 years of follow-up examinations is required, because the contralateral adrenal adenoma might have clinically significant endocrine function later[1,8]. Bilateral adenomas generally appear at the same time, but there has been a report of an adenoma appearing 9 years after the contralateral surgery[8]. In our case,the bilateral adenomas were both functioning; we resected the left one first because ofits thriving function on AVS. Three months later, we removed the right adenoma.When bilateral adrenal tumors are considered, a unilateral or bilateral adenoma resection is a better choice if functional adrenal tissue can be preserved to avoid acute adrenal insufficiency or lifelong steroid replacement. However, how much residual adrenal tissue is required for adequate adrenal function has not been much known[18].Brauckhoff estimated that preservation of approximately one-third of the entire adrenal gland could provide sufficient function[20]. Several authors have advocated preserving the adrenal vein, because adequate venous preservation may be important for maintaining the functionality of the remnant tissue[21,22]. But, in most cases,impaired adrenocortical function is likely caused by atrophy of the normal adrenal tissue. Few studies have demonstrated the feasibility of a partial adenomectomy for BAAs. Glucocorticoid therapy has to be employed to maintain the balance of water and electrolyte metabolism after surgery. Some studies have reported that long-term inadequate corticosteroid replacement therapy might provoke pituitary ACTHproducing hyperplasia adenoma[23-26]. Therefore, proper use of corticosteroids is significantly important. It has been suggested that corticosteroid replacement therapy can be divided into several doses (for example, it can be divided equally into three doses a day, taken at 9:00, 14:00, and 20:00 or 2/3 of a total dose in the morning and 1/3 in the early afternoon)[27].

Table 2 The results of peripheral 1-deamino-8-D-arginine-vasopressin stimulation test

Based on the reported cases, the clinical characteristics of BAAs could be summarized as: (1) Mainly occurring in mid-aged females; (2) Varying clinical symptoms, though most patients visit hospital because of typical symptoms; (3) Being a kind of ACTH-independent CS, with hypercortisolism, absence of serum cortisol diurnal rhythm, elevated UFC, and no suppression of serum cortisol after low-dose or high-dose dexamethasone suppression testing, while ACTH cannot be tested or is in the normal range, resulting in no reaction to the ACTH stimulation test; (4) Probably different pathological features and functioning state; (5) Bilateral well-encapsulated adenomas of 2.0 cm - 3.5 cm in diameter on the CT scan, with the presence of single or numerous nodules[19,28]; and (6) Normal findings of the MRI of the pituitary[19]. It has been reported that except for glucocorticoids, BAAs could also secrete mineralocorticoids and androgen[29]. In our patients, the plasma renin activity, the ALD concentration, the ALD-to-renin ratio, and the urine epinephrine and dopamine levels were in the normal range, while norepinephrine was only elevated slightly.

CONCLUSION

When patients present with bilateral adrenal lesions, it is crucial to make a definitive diagnosis before operation since various treatments are prescribed for different causes. Few cases of BAAs diagnosed using AVS have been reported. Our case indicates that AVS might be useful for obtaining differential diagnoses in such cases.Once considering BAAs, it is not recommended that bilateral adenomas be removed simultaneously. Hormone replacement therapy may be needed for fear of adrenal insufficiency, and the tapered discontinuation of the replacement therapy is necessarily slow.

Table 3 The results of bilateral adrenal vein sampling

Figure 2 Histological characteristics of the adenomas (Hematoxylin-eosin staining). A-D: The left (A: ×40, B: ×100) and right (C: ×40, D: ×100) adenomas comprised both clear cells and compact cells.

Figure 3 Immunohistochemical staining of the left adrenal adenoma (×100). A and B: Areas negative for chromogranin A (CgA) (A) and cytokeratin (CK) (B); CE: Tumor cells exhibiting strong staining for inhibin (C), synaptophysin (Syn) (D), and MelanA (E); F and G: Most parts of the tumor showed a proliferation index ＜ 2%(F) and spotty positivity for S100 (G).

Figure 4 Immunohistochemical staining of the right adrenal adenoma (×100). Areas negative for chromogranin A (CgA) (A) and cytokeratin (CK) (B), where some tumor cells exhibited positive staining for inhibin (C), synaptophysin (Syn) (D), and MelanA (E). Most parts of the tumor show a proliferation index ＜ 2% (F) and spotty positivity for S100 (G).

Figure 5 The timeline of this case report.

ACKNOWLEDGEMENTS

The authors thank all of the treatment groups of the Chinese People’s Liberation Army General Hospital.