- Case Report
- Open Access
Adrenalectomy for solitary adrenal metastasis from colorectal cancer: A case report
© Kosmidis et al; licensee BioMed Central Ltd. 2008
- Received: 25 June 2008
- Accepted: 18 July 2008
- Published: 18 July 2008
Patients with adrenal metastasis from various primary tumours are regarded as cases of diffuse systemic spread and considered unsuitable for surgical resection. We herein report an operable case of heterochronic adrenal metastasis from colorectal carcinoma in a 63-year-old woman.
Sixteen months after low anterior resection for the primary tumour, left lower pneumonectomy was performed for a solitary lung metastasis. Four months later a right adrenal metastasis was detected by magnetic resonance imaging (MRI), as sole evidence of metastatic disease. A right adrenalectomy was performed. The histopathological examination revealed adenocarcinoma compatible with the colorectal carcinoma resected 19 months earlier. The patient received adjuvant chemotherapy after each operation and is alive and free of disease 21 months after the adrenalectomy.
The possibility of adrenal metastasis should be considered in the follow-up of patients after primary surgery for colorectal cancer, even though other sites are the main metastatic sites. Although the prognosis of adrenal metastasis from colorectal cancer is poor, we suggest that patients with solitary adrenal metastasis may benefit from complete removal of it.
- Adrenal Gland
- Adrenal Mass
- Laparoscopic Adrenalectomy
Adrenal metastasis most commonly occurs in patients with lung, breast and renal cancer [1, 2]. In general, metastasis to the adrenal gland is regarded as an indicator of widespread disease, but in rare cases, isolated adrenal metastasis can be found [3–6]. Although the incidence varies among reports, it is generally accepted that adrenal metastasis from colorectal cancer (CRC) is relatively rare. As a result of recent advances in radiological noninvasive techniques, metastasis to the adrenal gland can be detected during follow up after primary operations for CRC. Whether isolated metastasis to the adrenal gland needs to be resected, remains controversial. Surgical resection of the involved adrenal gland seems to be able to provide a survival benefit for selected patients, according to several previously reported cases, whereas radiation and chemotherapy have relatively poor results for these lesions [1, 4, 7].
A 63-year-old-woman presented with lower abdominal pain and anal bleeding on defecation. Colonoscopy revealed intraluminal stenosis of the colorectal junction and biopsy specimens were obtained. Histologically, a well-differentiated adenocarcinoma was diagnosed. There was no evidence of metastasis, based on the results of abdominal computed tomography (CT) and chest X-ray, while (carcinoembryonic antigen) CEA was normal at 2.36 ng/ml. The patient underwent low anterior resection for CRC on 14 July 2004. The lesion was a stage Â2 (Astler-Coller) tumour, 3,0 × 2.5 cm in size, located in the rectosigmoid colon. Microscopic examination showed well-differentiated adenocarcinoma, penetrating the muscularis propria, without lymphatic and vascular invasion and without metastases to 15 dissected lymph nodes. According to the classification of TNM (tumour, lymph nodes, metastasis), the disease was stage II. Her postoperative course was uneventful, and she was started on adjuvant chemotherapy, comprised of oxaliplatin i.v., 85 mg/m2 (on day 1), leukovorin i.v., 200 mg/m2 (on days 1,2), 5 FU (fluorouracil) i.v., bolus 400 mg/m2 (on days 1,2), 5 FU i.v., 22 hours-infusion, 600 mg/m2 (on days 1,2), every 2 weeks for 12 cycles.
The patient is alive and free of disease 3 years and 4 months after the primary operation for CRC and 21 months after the right adrenalectomy.
The incidence of adrenal metastasis from CRC ranges from 0.15% to 17.4% with a mean percentage of 16%, according to different reports . By performing a medline literature search, we were able to identify 24 previously reported cases of resection of adrenal metastasis from CRC [1–9]. Five of these, including ours, had also lung metastasis either synchronous or metachronous [1–9]. It is conceived that a number of routes of adrenal metastasis from CRC exist, including systemic venous, portal venous, arterial, and lymphatic routes . Katayama et al. suggested that there is a route of hematogenous metastasis from the primary lesion via the lung to the adrenal gland . Thus, the significance of long-term follow-up after resection of CRC for early detection of adrenal metastasis, especially after resection of lung metastasis, should not be overlooked.
Patients' serum CEA levels are usually elevated when a metastasis is diagnosed, and CEA is considered to be useful for indicating the presence of adrenal metastasis after surgery for CRC . However, the serum level of CEA in our patient was normal despite the occurrence of lung and adrenal metastasis. Nevertheless, the ability to detect clinically silent adrenal metastasis has increased due to the widespread use of imaging modalities, including ultrasonography, CT and MRI. Therefore, in addition to measuring serum CEA, these modalities can be used in the follow up of patients who undergo a primary operation for CRC.
Adrenal metastasis from CRC is usually a part of systemic disease, accompanied by poor prognosis and has been regarded as having no indication for surgical resection [3, 4]. On the other hand, resection of solitary adrenal metastasis from CRC should be offered to patients with significant (> 6 months) disease free interval, since it may improve chances of survival [1, 3]. However, patients whose adrenal metastases are discovered synchronously or within 6 months of diagnosis of the primary tumour are less amenable to cure from metastasectomy. This may be due to the intrinsic biologic aggressiveness of the tumour and its metastases. Kim et al suggest that all metastases are present microscopically or macroscopically at the time of primary tumour diagnosis and that metastatic deposits which remain clinically undetectable beyond 6 months reflect the slow-growing nature of these tumours .
One could argue that it was the change in chemo regime rather than the surgical resection that helped the patient. In a recent review paper , Gundgaard et al reported median time to progression (mTTP) up to 7 months and a medium overall survival (mOS) of 16 months with third line chemotherapy. The highest mÔÔP, 9.8 months, was reported for the combination of cetuximab combined with irinotecan, the treatment our patient received.
It is difficult to determine whether adrenal metastasectomy has affected the natural history of our patient. However, it is evident that nonsurgical treatment of solitary adrenal metastases has been associated with poor survival. The small number of patients with isolated adrenal metastasis of colorectal carcinoma makes a randomized, prospective trial comparing surgical resection to other treatment modalities highly unlikely.
Laparoscopic adrenalectomy has rapidly replaced open adrenalectomy as the procedure of choice for benign adrenal tumours in the last decades. However, laparoscopic resection is controversial for large, potentially malignant adrenal tumours and necessitates experience in open surgery and advanced laparoscopic surgery . Therefore it is essential to differentiate benign and non-functional lesions from malignant or hormonally active ones so that appropriate treatment strategies can be initiated. In our case, since the adrenal mass was possibly malignant, we performed an open adrenalectomy.
Adrenal metastasis from CRC via the lung to the adrenal gland is considered to be relatively rare. It is generally accepted that a solitary adrenal metastasis from adenocarcinoma of the colon and rectum should be resected to achieve good prognosis. Therefore, it is important to consider the possibility of adrenal metastasis from CRC during follow-up after the primary operation. To detect adrenal metastasis early, radiological modalities such as US, CT and MRI as well as the measurement of serum CEA, should be done regularly. New modalities, such as (2-[18F] fluoro-2-deoxy-Dglucose (FDG) and positron emission tomography) 18F-FDG PET and (Computed Tomography-Positron Emission Tomography) CT-PET may offer better chances to detect clinically silent adrenal metastasis in the future.
Written informed consent was obtained from the patient for publication of this case report and any accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of the ≪Cases Journal≫.
- Kim SH, Brennan MF, Russo P, Burt ME, Goit DG: The role of surgery in the treatment of clinically isolated adrenal metastasis. Cancer. 1998, 82: 389-94. 10.1002/(SICI)1097-0142(19980115)82:2<395::AID-CNCR20>3.0.CO;2-T.View ArticlePubMedGoogle Scholar
- Murakami S, Terakado M, Hashimoto T, Tsuji Y, Okubo K, Hirayama R: Adrenal metastasis from rectal cancer: report of a case. Surg Today. 2003, 33: 126-30. 10.1007/s005950300028.View ArticlePubMedGoogle Scholar
- Katayama A, Mafune K, Makuuchi M: Adrenalectomy for solitary adrenal metastasis from colorectal carcinoma. Jpn J Clin Oncol. 2000, 30: 414-6. 10.1093/jjco/hyd104.View ArticlePubMedGoogle Scholar
- Komuro Y, Watanabe T, Kanazawa T, Tada T, Fukatsu K, Hosaka A, Hata K, Nagawa H: A case of adrenal metastasis from rectal carcinoma without lung metastasis: evaluation for alteration of loss of heterozygosity and immunohistochemical expression. J Gastroenterol. 2004, 39: 594-5. 10.1007/s00535-003-1351-0.View ArticlePubMedGoogle Scholar
- Nagakura S, Shirai Y, Nomura T, Hatakeyama K: Long-term survival after resection of colonic adenocarcinoma with synchronous metastases to the liver, adrenal gland and aortic-caval lymph nodes: report of a case. Dis Colon Rectum. 2002, 45: 1679-80. 10.1007/s10350-004-7258-x.View ArticlePubMedGoogle Scholar
- Des Guetz G, Montravers F, Spatzierer , Tabah I, Grahek D, Talbot JN, Bouillot JL, Pujade-Lauraine E: Isolated metastatic adrenal involvement with colon cancer and FDG coincidence detection imaging. Clin Nucl Med. 2003, 28: 238-10.1097/00003072-200303000-00019.PubMedGoogle Scholar
- Kanjo T, Albertini M, Weber S: Long-term disease-free survival after adrenalectomy for isolated colorectal metastases. Asian J Surg. 2006, 29: 291-3.View ArticlePubMedGoogle Scholar
- Kato T, Tsujie M, Handa R, Oshima S, Iijima S, Yamamoto H, Kurokawa E, Kikawa N: A case of rectal cancer with solitary adrenal metastasis. (Article in Japanese). Gan To Kagaku Ryoho. 2004, 31: 1699-701.PubMedGoogle Scholar
- Moreno-Elola A, Moreno-Gonzalez E, Alonso-Casado O, Meneu-Diaz JC, Garcia-Garcia I, Abradelo-Usera M: Exceptional bilateral adrenalectomy after secondaries from colorectal cancer. Hepatogastroenterology. 2004, 51: 103-5.PubMedGoogle Scholar
- Gundgaard MG, Soerensen JB, Ehrnrooth E: Third-line therapy for metastatic colorectal cancer. Cancer Chemother Pharmaco. 2008, 61: 1-13. 10.1007/s00280-007-0573-x.View ArticleGoogle Scholar
- Zografos GN, Markou A, Ageli C, Kopanakis N, Koutmos S, Kaltsas G, Piaditis G, Papastratis G: Laparoscopic surgery for adrenal tumours. A retrospective analysis. Hormones (Athens). 2006, 5: 52-6.View ArticleGoogle Scholar
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