Literature DB >> 21264083

Endogenous excess cortisol production and diabetes mellitus as predisposing factors for pulmonary cryptococcosis: a case report and literature review.

B Thangakunam1, D J Christopher, S Kurian, R Thomas, P James.   

Abstract

Pulmonary cryptococcosis usually occurs as an opportunistic infection in immunocompromised patients. Endogenous Cushing's syndrome is associated with cortisol excess and can predispose to development of cryptococcal infections. We report a case of diabetic patient with ACTH secreting pituitary tumour who developed a cavitating lung mass. Computed tomography-guided biopsy of the lesion revealed mucicarminophilic budding forms of cryptococcus. Broncheoalveolar lavage culture grew Cryptococcus neoformans. There was radiological response to treatment with liposomal Amphotericin, but patient ultimately succumbed to septicemia and multiorgan failure. Opportunistic infections with organisms like Cryptococcus neoformans, should be considered in patients with endogenous Cushing's syndrome and a pulmonary infiltrate.

Entities:  

Keywords:  Cortisol; Cryptococcosis; Cushing's syndrome; Diabetes mellitus; Pituitary

Year:  2008        PMID: 21264083      PMCID: PMC3019345          DOI: 10.4103/0970-2113.45281

Source DB:  PubMed          Journal:  Lung India        ISSN: 0970-2113


INTRODUCTION

Pulmonary cryptococcosis occurs usually in the immunocompromised patients. Excess cortisol production can theoretically produce an immunodeficiency state and predispose to cryptococcosis. We describe a diabetic patient with ACTH-producing pituitary tumour who developed pulmonary cryptococcosis.

CASE REPORT

A fifty-two year old bank manager, with history of systemic hypertension, Type II diabetes mellitus with nephropathy of eight years duration and ankylosing spondylosis of thirty-years duration, presented with history of decrease in vision and field defects in both eyes of two months duration. He had history of weight gain, proximal myopathy and easy bruisability. He subsequently developed altered behaviour in the form of irritability and periods of unresponsiveness. He was evaluated with MRI of brain, which showed a sellar mass (2.2x2x2.4 cm) with suprasellar extension extending into the right parasellar region encasing the cavernous segment of right internal carotid artery and impinging on optic chiasma (Fig I). Serum ACTH level at 8 am was 188 pg/mL (Normal 9–52pg/mL). Serum cortisol levels at 8 am and 6 pm was elevated, both being 72 µg/dL. His HIV serology was negative. His bone marrow examination was non-contributory.
Fig 1

Sagittal section of MRI brain showing pituitary tumour

Sagittal section of MRI brain showing pituitary tumour Subsequently, he developed breathing difficulty for which a chest radiograph was done which showed a cavitating mass in the posterior segment of left upper lobe (Fig II). Computed Tomography (CT) scan of chest confirmed the presence of this lesion and in addition revealed paratracheal and subcarinal lymphadenopathy. CT guided biopsy of the lung lesion was done, and it showed necrotic material infiltrated by few lymphocytes and mucicarminophilic budding forms of cryptococcus (Fig III). Fiberoptic bronchoscopy was normal and bronchoalveolar lavage culture grew Cryptococcus neoformans. In view of diabetic nephropathy, the patient was started on liposomal Amphotericin B (Ambisome) at a dose of 50mg on first day and then 150mg per day. He was unfit for surgical resection of the pituitary tumour. Ketoconazole at a dose of 400mg per day was started for control of hypercortisolism and continued for 22 days. Repeat chest radiograph after a cumulative dose of 950mg Ambisome showed decrease in size of the pulmonary lesion. However he developed Staphylococcus aureus bacteremia and multi-organ failure. He required endotracheal intubation and mechanical ventilation, on which he developed ventilator-associated pneumonia, refractory septic shock to which he succumbed.
Fig 2

Chest radiograph showing thick walled cavity left upper lobe

Fig 3

High power view of lung tissue with mucicarminophilic budding forms of cryptococcus

Chest radiograph showing thick walled cavity left upper lobe High power view of lung tissue with mucicarminophilic budding forms of cryptococcus

DISCUSSION

Cryptococcus neoformans is a ubiquitous fungus, being commonly found in bird droppings, soil and decayed wood. It causes opportunistic infections, predominantly in patients with T-cell-mediated immune defects, like those with AIDS and transplant-related immunosuppression123. Corticosteroid therapy, cancer chemotherapy, diabetes mellitus and hematological malignancies are also predisposing factors for the development of cryptococcal infections. The spectrum of disease caused by this fungus ranges from asymptomatic pulmonary colonization to life-threatening meningitis and overwhelming cryptococcemia. Pulmonary cryptococcosis in non-immunocompromised patients is rare and most of such cases resolve spontaneously3. In our patient the only risk factors for pulmonary cryptococcosis were endogenous Cushing's syndrome and diabetes mellitus. Endogenous Cushing's syndrome is associated with severe cortisol excess and can predispose to opportunistic infections. Pulmonary cryptococcosis in association with endogenous excess cortisol production is rare and only a few cases have been reported4–7 (Table No: I). In a case series of 143 patients with cryptococcosis who were HIV negative and not organ transplant recipients, only one patient had Cushing's disease as a risk factor3. Bakker et al described a patient with ACTH-dependent Cushing's syndrome whose clinical course was complicated by simultaneous infections with Pneumocystis carinii, Staphylococcus aureus, Candida albicans, Aspergillus fumigatus and Herpes simplex and which proved to be fatal8. Hypercortisolism associated with Cushing's syndrome appears to induce a transitory immune deficiency state and opens a window of opportunity for various infectious agents9.
Table I

Association of Pulmonary Cryptococcosis with Endogenous Cushing's syndrome reported in literature.

Author (year)Pulmonary Cryptococcosis - Diagnostic modalityType of Cushing's syndrome
Kramer M (1983)-ACTH dependent
Yamamoto N (1985)-ACTH dependent
Drew PA (1998)FNACACTH dependent
Takahashi S (2001)BALAdrenal tumour
Lacativa PG (2004)NecropsyACTH dependent
Association of Pulmonary Cryptococcosis with Endogenous Cushing's syndrome reported in literature. In non-AIDS patients cryptococcosis has also been associated with diabetes mellitus. In a series of 40 HIV-negative patients with cryptococcosis 14% had diabetes mellitus10. In another series of 22 patients with pulmonary cryptococcosis 7 had diabetes11. The recommended treatment for non-meningeal cryptococcosis in HIV negative individuals is Amphotericin B in severe disease and Fluconazole in mild disease. In those with meningeal forms combination therapy with Amphotericin and Flucytosine is essential. In our patient cerebrospinal fluid examination to rule out meningeal involvement could not be done, due to raised intra cranial pressure. In conclusion, patients with Cushing's syndrome or diabetes mellitus may be prone to infections including fungal infections such as with Cryptococcus neoformans. This should be kept in mind while evaluating such patients who develop pulmonary infections.
  11 in total

1.  Pulmonary cryptococcosis and pituitary Cushing's disease.

Authors:  P A Drew; K Takezawa
Journal:  Diagn Cytopathol       Date:  1998-05       Impact factor: 1.582

2.  Surveillance of cryptococcosis in Alabama, 1992-1994.

Authors:  C J Thomas; J Y Lee; L A Conn; M E Bradley; R W Gillespie; S R Dill; R W Pinner; P G Pappas
Journal:  Ann Epidemiol       Date:  1998-05       Impact factor: 3.797

3.  Cryptococcosis in human immunodeficiency virus-negative patients.

Authors:  Sasisopin Kiertiburanakul; Sirirat Wirojtananugoon; Roongnapa Pracharktam; Somnuek Sungkanuparph
Journal:  Int J Infect Dis       Date:  2005-11-09       Impact factor: 3.623

4.  [ACTH dependent Cushing's syndrome with an empty sella turcica: report of three cases with emphasis on diagnostic value of selective venous sampling].

Authors:  N Yamamoto; M Negoro; T Yokoe; K Ichihara; T Nakane; A Kuwayama; N Kageyama
Journal:  No Shinkei Geka       Date:  1985-12

Review 5.  Functioning adrenal black adenoma with pulmonary and cutaneous cryptococcosis: a case report and review of English literature.

Authors:  S Takahashi; H Iijima; Y Moriwaki; T Yamamoto; S Matsuoka; Z Tsutsumi; M Nojima; A Kubota; T Hada
Journal:  J Endocrinol Invest       Date:  2001-11       Impact factor: 4.256

6.  Clinical features and high-resolution CT findings of pulmonary cryptococcosis in non-AIDS patients.

Authors:  Kazuma Kishi; Sakae Homma; Atsuko Kurosaki; Tadasu Kohno; Noriko Motoi; Kunihiko Yoshimura
Journal:  Respir Med       Date:  2005-10-18       Impact factor: 3.415

7.  [Pseudotumoral pulmonary cryptococcosis in association with Cushing's syndrome].

Authors:  Paulo G S Lacativa; Ines Donangelo; Márcia B Wagman; Lino Sieiro Neto; Carolina R Caldas; Alice H D Violante; Roberto J Lima; Mário Vaisman
Journal:  Arq Bras Endocrinol Metabol       Date:  2004-07-07

8.  Pulmonary cryptococcosis in nonimmunocompromised patients.

Authors:  Hassan F Nadrous; Vera S Antonios; Christine L Terrell; Jay H Ryu
Journal:  Chest       Date:  2003-12       Impact factor: 9.410

9.  Pulmonary cryptococcosis and Cushing's syndrome.

Authors:  M Kramer; M L Corrado; V Bacci; A C Carter; S H Landesman
Journal:  Arch Intern Med       Date:  1983-11

10.  Cushing's syndrome complicated by multiple opportunistic infections.

Authors:  R C Bakker; P R Gallas; J A Romijn; W M Wiersinga
Journal:  J Endocrinol Invest       Date:  1998-05       Impact factor: 4.256

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.