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DOI:10.2214/AJR.08.1166
AJR 2009; 192:300-301
© American Roentgen Ray Society


Radiologic-Pathologic Conferences of the University of Texas M. D. Anderson Cancer Center

Adrenal Pheochromocytoma with Surrounding Brown Fat Stimulation

Revathy B. Iyer1, Charles C. Guo2 and Nancy Perrier3

1 Division of Diagnostic Imaging, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Blvd., Box 57, Houston, TX 77030.
2 Division of Pathology, The University of Texas M. D. Anderson Cancer Center, Houston, TX.
3 Division of Surgical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, TX.

Received May 5, 2008; accepted after revision July 17, 2008.

Address correspondence to R. B. Iyer (riyer{at}mdanderson.org).

Keywords: adrenal gland • brown fat • FDG PET/CT • pheochromocytoma

A 62-year-old woman with a history of poorly controlled hypertension and anxiety presented with abdominal pain and a hypertensive crisis. Abdominal imaging revealed a 3.5-cm right adrenal mass. A 24-hour urinary collection revealed markedly elevated catecholamines (particularly norepinephrine, which was 774 µg/24 hr [normal, 15-100 µg/24 hr]), confirming the diagnosis of pheochromocytoma.

Dedicated adrenal CT showed an approximately 3.5-cm enhancing mass in the right adrenal gland with central low attenuation and significant soft-tissue stranding in the surrounding fat. Whole-body 18F-FDG PET showed intense uptake of the mass as well as the surrounding retroperitoneal tissues, with a maximum standardized uptake value of approximately 20 extending into the mediastinum (Fig. 1A). The patient received {alpha}- and β-blockers in preparation for surgery. Repeat abdominal CT was performed and revealed a decrease in the previously seen retroperitoneal stranding (Figs. 1B and 1C). The patient was taken to the operating room and underwent a right adrenalectomy. Gross sections revealed a 3.8-cm well-circumscribed tan-yellow tumor in the adrenal gland. Microscopically, the tumor cells were arranged in solid or alveolar patterns and surrounded by a capillary-rich framework (Fig. 1D). The cytoplasm was amphophilic with a fine granular texture, and the nuclei were round to ovoid with a single prominent nucleolus. The surrounding adipose tissue was composed of multivacuolated and univacuolated cells with increased vascularity. The final pathologic diagnosis was pheochromocytoma with surrounding brown fat (Fig. 1D).


Figure 1
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Fig. 1A —62-year-old woman with predominantly norepinephrine-producing adrenal pheochromocytoma. Coronal 18F-FDG PET maximum-intensity-projection image shows intense uptake in retroperitoneum extending to mediastinum (arrow).

 

Figure 2
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Fig. 1B —62-year-old woman with predominantly norepinephrine-producing adrenal pheochromocytoma. Contrast-enhanced CT scan shows right adrenal mass (black arrow) with significant stranding in surrounding fat (white arrow).

 

Figure 3
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Fig. 1C —62-year-old woman with predominantly norepinephrine-producing adrenal pheochromocytoma. Unenhanced CT scan after administration of {alpha}- and β-adrenergic blockers shows significant decrease in stranding in surrounding fat (arrow).

 

Figure 4
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Fig. 1D —62-year-old woman with predominantly norepinephrine-producing adrenal pheochromocytoma. Photomicrograph of tumor cells shows pheochromocytoma and surrounding brown fat. Pheochromocytoma cells are arranged in solid patterns with amphophilic cytoplasm and round nuclei (white arrow). Brown fat is composed of multivacuolated and univacuolated cells with increased vascularity (black arrow). (H and E, x100)

 
Pheochromocytoma is an uncommon neoplasm that originates from chromaffin cells and may arise in the adrenal medulla (90%) or in extraadrenal locations (10%). Pheochromocytomas induce hypertension through the production of catecholamines, primarily epinephrine, and, less commonly, norepinephrine. Pheochromocytomas are typically sporadic and solitary neoplasms [1]. Only a small percentage of patients with hypertension have a pheochromocytoma, but in those who do, complete resection of the functional tumor provides cure. Cross-sectional imaging such as CT or MRI is an excellent study for showing adrenal masses.

Brown fat is normally present in fetuses and infants and diminishes in adults to account for only 1% of the total body mass. Brown fat may have a metabolic or a thermoregulatory function. Remnants of brown fat in the adult are usually found in the neck, mediastinum, axilla, retroperitoneum, and abdominal wall [2]. Brown adipose tissue has much more sympathetic noradrenergic innervation than white adipose tissue [3]. Norepinephrine also has a regulatory function in brown fat. Catecholamine stimulation increases the number of brown fat cells, stimulates lipolysis and glucose transport, and uncouples protein-1 expression in brown fat cells, resulting in heat production [3].

Brown fat is frequently an incidental finding on FDG PET that may result in false-positive findings [4]. Careful correlation with coregistered CT images should be performed to exclude any masses in areas of brown fat uptake. After injection of the radiotracer, as patients wait to be imaged, controlled room temperature is important to prevent thermogenesis and increased brown fat stimulation. In patients with adrenergic stimulation due to excess catecholamine production, brown adipose tissue may be more abundant than in normal adults. The localization of FDG in areas of excess brown fat in these patients likely results from increased glucose transport related to norepinephrine excess [3, 5].

When interpreting examinations in patients with pheochromocytoma, the radiologist should bear in mind that FDG uptake may be increased in these patients because of the high circulating levels of norepinephrine. The dramatic FDG uptake in the surrounding retroperitoneal regions may make it difficult to resolve the pheochromocytoma from the surrounding brown fat with PET alone; PET/CT fusion is particularly helpful in this regard. In this patient, after administration of {alpha}-adrenergic and β-blockers, the extent of hypervascularity in the retroperitoneal fat decreased. Although follow-up PET was not performed, it is postulated that brown fat activity on FDG PET would also have decreased, as has been shown previously [5].

References

  1. Heaton JM. The distribution of brown adipose tissue in the human. J Anat 1972;112:35 -39[Medline]
  2. Medicow MM. One hundred cases of pheochromocytoma (107 tumors) at the Columbia-Presbyterian Medical Center, 1926-1976: a clinicopathological analysis. Cancer1977; 40:1987 -2004[CrossRef][Medline]
  3. Hadi M, Chen CC, Whatley M, Pacak K, Carrasquillo JA. Brown fat imaging with (18)F-6-fluorodopamine PET/CT, (18)F-FDG PET/CT, and (123) I-MIBG SPECT: a study of patients being evaluated for pheochromocytoma. J Nucl Med 2007;48:1077 -1083[Abstract/Free Full Text]
  4. Yeung HW, Grewal RK, Gonen M, Schoder H, Larson SM. Patterns of 18F FDG uptake in adipose tissue and muscle: a potential source of false-positives for PET. J Nucl Med2003; 44:1789 -1796[Abstract/Free Full Text]
  5. Ramacciotti C, Schneegans O, Lang H, et al. Diffuse uptake of brown fat on computed-tomography coupled positron emission tomoscintigraphy (PET-CT) for the exploration of extra-adrenal pheochromocytoma. Ann Endocrinol 2006;67:14 -19[Medline]

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