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18 December 2020: Articles  Japan

Masked Diabetes Insipidus Hidden by Severe Hyponatremia: A Case of Pituitary Metastasis of Lung Adenocarcinoma

Unusual clinical course, Challenging differential diagnosis, Unusual or unexpected effect of treatment, Diagnostic / therapeutic accidents, Adverse events of drug therapy , Educational Purpose (only if useful for a systematic review or synthesis)

Miki Watanabe1ABCDEF, Junichi Yasuda1CDEF, Kenji Ashida1ABCDEF*, Yuko Matsuo1CDE, Ayako Nagayama1CDE, Yuka Goto1CDE, Shimpei Iwata1CDE, Masayuki Watanabe2CDE, Jun Sasaki2BCDE, Tomoaki Hoshino2CDE, Masatoshi Nomura3ACDEF

DOI: 10.12659/AJCR.928113

Am J Case Rep 2020; 21:e928113

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Abstract

BACKGROUND: Hyponatremia is an electrolyte disorder frequently encountered by clinicians. Secondary adrenal insufficiency due to pituitary metastatic tumors should be considered as an alternative diagnosis when clinicians encounter patients with lung cancer who demonstrate hyponatremia. However, masked central diabetes insipidus should also be considered to prevent critical dehydration when glucocorticoid replacement therapy will be initiated.

CASE REPORT: A 70-year-old man with advanced lung adenocarcinoma demonstrated high-grade hyponatremia of 122 mmol/L. Magnetic resonance imaging disclosed a metastatic pituitary tumor and endocrinological examinations confirmed panhypopituitarism, including secondary adrenal insufficiency. Hydrocortisone replacement revealed masked diabetes insipidus with elevation of serum sodium levels that reached 151 mmol/L. Desmopressin administration was required to prevent water depletion and to immediately ameliorate the hypernatremia.

CONCLUSIONS: This is the first case report of masked diabetes insipidus that demonstrated high-grade hyponatremia. Secondary adrenal insufficiency can mask the hypernatremia that is a typical manifestation of diabetes insipidus. Physicians should consider adrenal insufficiency and diabetes insipidus due to pituitary metastasis of advanced malignancies, even when they encounter patients with hyponatremia.

Keywords: Diabetes insipidus, adrenal insufficiency, Glucocorticoids, Hyponatremia, Pituitary Neoplasms, Adenocarcinoma of Lung, Aged, Diabetes Mellitus

Background

Metastatic pituitary tumors are observed in approximately 0.1% to 28% of autopsy cases with various malignancies [1]. Among the various malignancies, lung cancer is a common source of metastatic pituitary tumors [1–3]. Actually, approximately 1% of the cases with pituitary tumors in whom transsphenoidal hypophysectomy was performed had metastatic pituitary tumors [1]. In this context, physicians should not overlook occult pituitary metastasis, even when the various symptoms of advanced malignant diseases have cloaked it.

Metastasis is more likely to occur in the posterior lobe than in the anterior lobe of the pituitary gland because the posterior lobe is fed by the pituitary artery, whereas the latter is fed by the pituitary portal vein [2]. Thus, posterior lobe function tends to be disturbed compared with anterior lobe functions. Disturbances of antidiuretic hormone (ADH), adrenocortico-tropic hormone (ACTH), thyroid-stimulating hormone (TSH), gonadotropins (luteinizing hormone [LH] and follicle-stimulating hormone [FSH]), and prolactin (PRL) are observed in 59%, 49%, 57%, 70%, and 83% of patients, respectively, with metastatic pituitary tumors. In contrast, few patients with pituitary adenoma exhibit diabetes insipidus, whereas 26%, 14%, and 49% of them have disturbances in ACTH, TSH, and gonadotropins, respectively [4]. Thus, diabetes insipidus, visual disturbance, symptoms of anterior lobe disturbance, disturbed eye movement, head or eye pain, and general fatigue are frequently observed in patients with metastatic pituitary tumors [1,2,5].

Hyponatremia is an electrolyte disorder that physicians frequently encounter [6,7]. Patients with lung cancer may develop hyponatremia because of 2 endocrinological issues: high intrathoracic pressure-induced syndrome of inappropriate secretion of ADH (SIADH) [8,9] and primary [10] or secondary [10,11] adrenal insufficiency owing to metastatic tumor. With regard to pituitary metastasis, it remains unclear whether patients who have both secondary adrenal insufficiency and central diabetes insipidus because of metastatic tumor could demonstrate hyponatremia.

Here, we report the case of a patient with secondary adrenal insufficiency complicated by central diabetes insipidus because of pituitary metastasis of lung adenocarcinoma. This is the first case report of a patient who demonstrated severe hyponatremia in that condition. Of note, we describe the remarkable changes in serum sodium concentration during the patient’s clinical course. Physicians should be aware of and not overlook this unique condition when they encounter hyponatremia with advanced malignancies.

Case Report

A 70-year-old man was admitted to our hospital complaining of anorexia and hyponatremia during chemotherapy for lung cancer. He had developed lung adenocarcinoma (Figure 1) at the age of 65 and underwent left upper lobectomy. Recurrence in the lung and multiple brain metastases were revealed by computed tomography (CT) and magnetic resonance imaging (MRI), respectively, 16 months prior to the admission, but no abnormalities were noted in the pituitary gland. Gamma knife radiotherapy for the brain metastases and chemotherapy using erlotinib were started. However, exacerbation of the brain metastases was observed with progression of hyponatremia and malaise.

Severe hyponatremia of 122 mmol/L was noted at his first admission on April 27, 2018 (Table 1). Initially, hyponatremia due to anorexia was considered; thus, 6 g/day of sodium chloride was administrated orally and 500 mL/day of saline intravenously. The serum sodium level increased to 135 mmol/L on May 2, 2018, and he was discharged from the hospital; however, the hyponatremia reappeared. SIADH was also considered because of the preserved urinary sodium level (41 mmol/mL) and the high osmolality of the urine compared with the low osmolality of the plasma; however, further examinations of endocrine function disclosed a decrease in the levels of ACTH, FSH, LH, and TSH (Table 1). Additionally, MRI revealed pituitary metastasis of the lung adenocarcinoma (Figure 2). We could not assess the high-intensity signal in T1-weighted image of the posterior lobe because of restricted availability of enhanced imaging and severe plasma hypoosmolality. Thus, we diagnosed panhypopituitarism, and 20 mg/day of hydro-cortisone and 50 μg/day of levothyroxine were administered for replacement therapy (Figure 3).

Notably, the hyponatremia was immediately improved and the serum sodium concentration increased from a low level to a high level of 151 mmol/L (Figure 3). Low serum ADH level, high plasma osmolality, low urine osmolality (Table 2), and polyuria with an increased number of urinations (up to 18 times/day) were present; daily urine volumes were not recorded. These findings indicated central diabetes insipidus due to a meta-static pituitary tumor, which had become apparent with corticosteroid administration. Oral desmopressin administration ameliorated the polyuria, increased the urine osmolality, and decreased the serum sodium concentration. Although the panhypopituitarism and diabetes insipidus were regulated by medications, the patient died because of progression of the lung adenocarcinoma 5 months after the first admission.

Discussion

We described a patient with lung cancer and pituitary metastasis who demonstrated notable changes in serum sodium concentration during his clinical course. This case report demonstrates 2 clinically important issues. First, masked diabetes insipidus can present as severe hyponatremia when complicated by adrenal insufficiency. Second, reevaluation of head MRI is required to detect the occult adrenal insufficiency caused by the pituitary metastasis. Precise evaluation and hormone replacements are required to provide better quality of life (QOL) and prognosis for patients with advanced malignancies.

Masked diabetes insipidus should be considered even when corticosteroid replacement therapy is applied to a patient with secondary adrenal insufficiency exhibiting severe hyponatremia. Diabetes insipidus ordinarily features hyperosmotic hypernatremia, reflecting the deficit of free water [3,7]. There has been no previous case report of diabetes insipidus that showed hyponatremia <130 mmol/L [2,3,5], although a low-normal serum sodium level of masked diabetes insipidus caused by central nervous system sarcoidosis has been reported [12]. Endocrinological examination suggested secondary adrenal insufficiency, secondary hypothyroidism, hypogonadotropic hypogonadism, and growth hormone deficiency in this case. MRI revealed a dumbbell-type tumor of the pituitary gland with suprasellar extension. Corticosteroid replacement led to an increase in urination that probably indicated polyuria, a decrease in the plasma ADH level, and an increase in the serum sodium concentration. Adrenal insufficiency, which has been suggested to induce hyponatremia through a decrease in miner-alocorticoid activity, impaired renal free-water clearance, and a relative increase in ADH secretion, can mask diabetes insipidus [2,5,12]. In this context, although corticosteroid replacement therapy rapidly ameliorates the adrenal insufficiency-related disorders [13], masked diabetes insipidus can be revealed with corticosteroid administration [5,12]. This study alerts physicians that masked diabetes insipidus can develop even in a patient with hypoosmotic hyponatremia.

Reevaluation of head MRI is required to detect the occult adrenal insufficiency due to the pituitary metastasis that is hidden behind the advanced malignancies. Patients with advanced malignancies often have general malaise, appetite loss, and nausea, and these are the major complaints of adrenal insufficiency and hyponatremia [14]. Secondary adrenal insufficiency may show few signs allowing recognition of the abnormality [14], whereas primary adrenal insufficiencies give clues to their diagnosis, including changes in skin pigmentation and elevated plasma ACTH concentrations [15]. Simultaneous evaluation of plasma ACTH paired with serum cortisol is required; however, at baseline, both values are insufficient to establish a diagnosis of secondary adrenal insufficiency in most cases. Further evaluations using stimulations with corticotropin-releasing hormone and/or ACTH are required to confirm the presence of secondary adrenal insufficiency [16]. Patients with metastatic pituitary tumors frequently develop diabetes insipidus, which can also mask the hyponatremia due to adrenal insufficiency [5]. Reevaluation by head MRI of patients with advanced malignancies was suggested to be beneficial to guide proper diagnosis.

Precise evaluation and replacement may be required to provide better QOL and prognosis for patients with advanced malignancies. Advances in chemotherapies, including molecular- and immune-targeting drugs, have recently improved the prognosis of various malignancies [17]. However, these beneficial drugs also have endocrinological adverse reactions [18,19]. Additionally, various malignancies, especially lung carcinoma, have a high frequency of pituitary metastasis. In this context, physicians should evaluate the pituitary functions of patients with lung cancer to avoid critical conditions.

Conclusions

Masked diabetes insipidus should be considered even in a patient with severe hypoosmotic hyponatremia. Pituitary metastasis should not be overlooked, while cachexia of advanced malignancies may mask the adrenal insufficiency. Reevaluation of the head MRI is required to detect occult pituitary metastasis. Precise evaluation and replacement therapy may provide better QOL and prognosis for patients with advanced malignancies.

References:

1.. Komninos J, Vlassopoulou V, Protopapa D, Tumors metastatic to the pituitary gland: Case report and literature review: J Clin Endocrinol Metab, 2004; 89; 574-80

2.. Javanbakht A, D’Apuzzo M, Badie B, Salehian B, Pituitary metastasis: A rare condition: Endocr Connect, 2018; 7(10); 1049-57

3.. Sirinvaravong S, Vibhatavata P, Chunharojrith P, Diabetes insipidus and panhypopituitarism as a first presentation of silent adenocarcinoma of lung: A case report and literature review: BMC Endocr Disord, 2019; 19(1); 114

4.. Al-Aridi R, El Sibai K, Fu P, Clinical and biochemical characteristic features of metastatic cancer to the sella turcica: An analytical review: Pituitary, 2014; 17(6); 575-87

5.. Castle-Kirszbaum M, Goldschlager T, Ho B, Twelve cases of pituitary metastasis: A case series and review of the literature: Pituitary, 2018; 21(5); 463-73

6.. Hoorn EJ, Zietse R, Diagnosis and treatment of hyponatremia: Compilation of the guidelines: J Am Soc Nephrol, 2017; 28(5); 1340-49

7.. Muhsin SA, Mount DB, Diagnosis and treatment of hypernatremia: Best Pract Res Clin Endocrinol Metab, 2016; 30(2); 189-203

8.. Gulsin GS, Jacobs MLB, Gohil S, Competing interests in a lung cancer with metastasis to the pituitary gland: syndrome of inappropriate ADH secretion versus diabetes insipidus: Oxf Med Case Reports, 2016; 2016(6); 125-29

9.. Fiordoliva I, Meletani T, Baleani MG, Managing hyponatremia in lung cancer: Latest evidence and clinical implications: Ther Adv Med Oncol, 2017; 9(11); 711-19

10.. Chabre O, Goichot B, Zenaty D, Bertherat J, Group 1. Epidemiology of primary and secondary adrenal insufficiency: prevalence and incidence, acute adrenal insufficiency, long-term morbidity and mortality: Ann Endocrinol, 2017; 78(6); 490-94

11.. Atallah-Yunes SA, Clark J, Samanani S, Soe M, Small cell lung cancer with pituitary metastasis presenting as secondary adrenal insufficiency: A case report and literature review: Am J Case Rep, 2019; 20; 207-11

12.. Non L, Brito D, Anastasopoulou C, Neurosarcoidosis-associated central diabetes insipidus masked by adrenal insufficiency: BMJ Case Rep, 2015; 2015 : bcr2014206390

13.. Carvalho F, Louro F, Zakout R, Adrenal Insufficiency in Metastatic Lung Cancer: World J Oncol, 2015; 6(3); 375-77

14.. Martin-Grace J, Dineen R, Sherlock M, Thompson CJ, Adrenal insufficiency: Physiology, clinical presentation and diagnostic challenges: Clinica Chim Acta, 2020; 505; 78-91

15.. Tallis PH, Rushworth RL, Torpy DJ, Falhammar H, Adrenal insufficiency due to bilateral adrenal metastases – a systematic review and meta-analysis: Heliyon, 2019; 5(5); e01783

16.. Crowley RK, Argese N, Tomlinson JW, Stewart PM, Central hypoadrenalism: J Clin Endocrinol Metab, 2014; 99(11); 4027-36

17.. Hirsch FR, Scagliotti GV, Mulshine JL, Lung cancer: Current therapies and new targeted treatments: Lancet, 2017; 389(10066); 299-311

18.. Kitajima K, Ashida K, Wada N, Isolated ACTH deficiency probably induced by autoimmune-related mechanism evoked with nivolumab: Jpn J Clin Oncol, 2017; 47(5); 463-66

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American Journal of Case Reports eISSN: 1941-5923
American Journal of Case Reports eISSN: 1941-5923