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 ¤ Introduction
 ¤ Patients and Methods
 ¤ Results
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 Table of Contents     
ORIGINAL ARTICLE
Year : 2021  |  Volume : 17  |  Issue : 1  |  Page : 76-80
 

Laparoscopic adrenalectomy for giant adrenal tumours: Technical considerations and surgical outcome


Department of Emergency, Emergency Surgery Unit, Careggi University Hospital, Florence, Italy

Date of Submission07-Nov-2019
Date of Decision25-Nov-2019
Date of Acceptance27-Jan-2020
Date of Web Publication24-Feb-2020

Correspondence Address:
Dr. Alessio Giordano
Emergency Surgery Unit, Careggi University Hospital, Largo Brambilla 3, 50134, Florence
Italy
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jmas.JMAS_266_19

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 ¤ Abstract 

Background: Giant adrenal tumours are tumours with size ≥6 cm. These are rare cancer associated with malignancy in 25% of cases.
Patients and Methods: A retrospective review was conducted on the medical records of patients admitted to our high-volume centre of Careggi University Hospital with a giant adrenal tumour and submitted to adrenalectomy between January 2008 and December 2018. The group of patients who underwent to laparoscopic adrenalectomy was compared with a group of patients that was submitted to open adrenalectomy.
Results: In the past 10 years, we performed about 245 adrenalectomies for benign and malignant adrenal tumours. Fifty (20.4%) of these were giant tumours. The medium size was 9.9 cm (7–22 cm). The mean age was 57 years (21–81 years). Thirty-four (68%) of these cancers were laparoscopically removed and 16 (32%) with an open approach. The surgical outcomes in these patients were optimal if compared to the group of patients submitted to open approach in terms of good pain control, hospital stay, mean operative time and bloodless. No difference was observed about post-operative complications in the two groups. The follow-up after 30 months for malignant tumours did not show local recurrences.
Conclusion: Our results pinpoint the advantages of performing a laparoscopic adrenalectomy for giant adrenal tumours. The tumour size is only a predictive parameter of possible malignancy, and the laparoscopic approach is a safe and feasible method in terms of surgical and oncological, only if performed by expert surgeons and in high-volume centres.


Keywords: Adrenal, giant adrenal tumour, laparoscopic adrenalectomy, laparoscopic surgery, open adrenalectomy


How to cite this article:
Giordano A, Alemanno G, Bergamini C, Valeri A, Prosperi P. Laparoscopic adrenalectomy for giant adrenal tumours: Technical considerations and surgical outcome. J Min Access Surg 2021;17:76-80

How to cite this URL:
Giordano A, Alemanno G, Bergamini C, Valeri A, Prosperi P. Laparoscopic adrenalectomy for giant adrenal tumours: Technical considerations and surgical outcome. J Min Access Surg [serial online] 2021 [cited 2021 Jan 24];17:76-80. Available from: https://www.journalofmas.com/text.asp?2021/17/1/76/279123



 ¤ Introduction Top


Laparoscopic adrenalectomy (LA) is actually considered the gold standard for the treatment for benign adrenal tumours. Since the first description performed by Gagner et al. in 1992,[1] some retrospective studies have confirmed that laparoscopic approach is associated with a decrease of the perioperative morbidity, lower complication rates, less operative blood loss, less post-operative pain and shorter hospital stay compared with open approach. Incidental adrenal tumours are relatively common, and adrenalectomy represents the third most commonly performed endocrine surgical procedure.[2] In literature, giant adrenal tumours (GAT) are defined as adrenal masses larger than 6 cm.[3] The overall incidence of adrenal tumours that require resection is exceedingly low and for this reason, GAT are considered rare, with an incidence ranging from 8.6% to 38.6% of all adrenal tumours.[4] In large adrenal tumour, it is detriment an accurate pre-operative study to assess the eventual malignancy of the lesion. Laparoscopy in case of GAT requires an accurate dissection to avoid capsular disruption, especially in case of malignancy. The incidence of malignancy in patients with GAT ranges from 10% to 53% with a consensus of 25%,[5] however, there are no evidence that suggests that a laparoscopic approach is contraindicated for GAT because the size is only a predictor factor of malignancy.[6] In this article, we report a 10 years' experience of LA for GAT.


 ¤ Patients and Methods Top


In our general and emergency surgery unit, between January 2008 and December 2018, 245 patients underwent surgery for adrenal tumour. Among these patients, 50 (20.4%) had GAT (with an adrenal mass larger than 6 cm). Demographic data were retrospectively collected from medical records.

Pre-operative evaluation

A multidisciplinary pre-operative study of all adrenal masses, especially of GAT, is mandatory. All patients were assessed by an accurate clinical evaluation, a hormonal assessment and an anatomical and functional imaging. To define the characteristics and size of the lesions, all patients were preoperatively submitted to abdominal magnetic resonance imaging or computed tomography (CT) scan. The only size of the lesion was not considered as a signal of malignant lesion.[7] The diagnosis of possible adrenal carcinoma was based, in fact, on the patient's history and radiologic findings as local infiltration, irregular margins or tumour heterogeneity, vascular invasion. In cases suspected for pheochromocytoma metaiodobenzylguanidine scintigraphy or positron emission tomography with FDOPA –CT scan (6-[18F]-L-fluoro-L-3, 4-dihydroxyphenylalanine) were performed. Complete hormonal tests were performed to identify functioning tumours. All patients with a pre-operative diagnosis of pheochromocytoma received specific pre-operative preparation. Indications for adrenalectomy included: hormone-secreting tumours (Cushing's lesion, aldosteronoma and pheochromocytomas) and all non-functioning tumours >4 cm.[8]

Surgical technique

All surgical operations were performed at our care centre unit by experienced laparoscopic surgeons in adrenal surgery. Laparoscopic adrenalectomies were performed using the lateral transperitoneal approach. Patients were placed in a lateral decubitus position with the affected side up. This approach allows a wider surgical workspace with an excellent exposure of the upper retroperitoneum, good control of vascular structure if compared to other approaches.[9] For the right adrenalectomy, we used four trocars in the right subcostal region, instead, for left-sided resection, we used three trocars in the left subcostal region. On the left-sided adrenalectomy, we used always fibrin glue for repositioning splenic-pancreatic block. One drainage was routinely used in all operations. At the end of the procedure, the large tumours were positioned in endobag device and removed with a subcostal mini-laparotomy. During the procedures, all tumours were handled with care, especially in cases of pheochromocytoma or carcinoma. No retroperitoneoscopic approach was performed. Open adrenalectomy (OA), with a transabdominal approach, was performed in cases with radiological findings of local invasion of the periadrenal fat tissue. [Figure 1] shows a case of giant adrenal carcinoma removed with a laparoscopic approach.
Figure 1: A case of giant adrenal tumour removed with laparoscopic approach

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Post-operative evaluation

All patients were transferred to a recovery room for the first 4–6 h after surgery, to monitor their blood pressure.

The Clavien-Dindo system was used for grading complications which occur as a result of surgical procedures.

Follow-up

Patients were checked in our outpatient clinic 1 week after the discharge. The follow-up protocol included the possibility of an on-call activation of our surgical team in case of adverse abdominal symptoms.

Statistical analysis

Data were expressed as a mean ± standard deviation. Statistical analyses were performed with the Chi-square test, Fisher's exact test or t-test. Statistical significance was set at P < 0.05, and resulting P values were adjusted according to the Bonferroni correction method. Data were analysed using the SPSS statistical software, IBM® (New York, United States).

Compliance with ethical standards

This retrospective study is in accordance with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. This article does not contain any studies with animals performed by any of the authors.


 ¤ Results Top


In the period of the study, between January 2008 and December 2018, 50 (20.4%) out of 245 patients referred to our centre for adrenal tumours presented with GAT. Thirty-four of these patients (68%) were submitted to LA, and 16 (32%) were submitted to OA. The population of the study was characterised by 28 males and 22 females with a mean age of 57 years (range: 21–81 years). For 24 patients (48%), the GAT was found incidentally, however, other clinical presentation included hypertension, abdominal pain or oncological work-up. Twenty-four patients (48%) presented with a functioning tumours, in particular, 15-secreting catecholamines (62.5%), 6 cortisol (25%), 2 aldosterone (8.3%) and 1 androgen (4.2%). The general characteristics of the population of the study are reported in [Table 1].
Table 1: General characteristics of 50 patients with giant adrenal tumours

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OA was indicated due to radiological characteristics or suspicion of local invasion (seven cases). In particular, during OA, it was necessary to remove ipsilateral kidney in four patients, spleen with pancreatic tail in one patient and lateral patches of the inferior vena cava in two patients due to local invasion. Whatever type of resection, the mean operative time was longer by an open approach (170 min, range: 140–200 min) than by laparoscopy (110 min, range: 75–130 min) (P = 0.043). Two of 34 patients submitted to LA were converted to OA: one for tenacious adhesions on the right side and one for important bleeding from inferior vena cava. A previous abdominal surgery was not an absolute contraindication for an LA. In all patients submitted to surgery for GAT, the tumour was excised through en bloc resection, and there was no capsular disruption during dissection.

The mean tumour size was 9.9 cm (range: 7–22 cm), and the lesions were localised on the right side in 24 patients and on the left side in 26 patients. We did not observe bilateral adrenal masses. The mean blood loss was 90 ml (range: 60–185 ml) for LA versus 210 ml for OA (range: 170–520 ml), (P = 0.037). The mean post-operative hospital stay for LA was 3 days (range: 2–5 days) versus 7 days (range: 5–14 days) for OA (P = 0.039). In the LA group, we did not observe any post-operative complication, whereas in the OA group, we have observed pulmonary infection in one patient, atrial fibrillation pharmacologically treated in one patient and post-operative anaemia that required blood transfusion in one patient (P = 0.082), as reported in [Table 2]. We did not observe any cases of major complications required surgical, radiological or endoscopic intervention (Dindo III); life-threatening complications required intensive care (Dindo IV) or death (Dindo V).
Table 2: Results of laparoscopic adrenalectomy versus open approach

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Twenty-seven tumours (54%) were malignant (15/34 LA treatment and 12/16 OA treatment), particularly 17 were adrenal carcinoma (34%), five were adrenal metastasis secondary to lung and breast cancer (10%), four were pheochromocytomas (8%) and one was a lymphoma (2%). Benign GATs (46%) included five adenomas (10%), 11 benign pheochromocytomas (22%), four myelolipomas (8%) and three endothelial cysts (6%). The median follow-up for malignant GAT was about 30 months (range: 6–48 months). No local recurrence and portside metastasis were noticed.


 ¤ Discussion Top


LA is today considered as the gold standard treatment for benign adrenal tumours. Since the first description in 1992 by Gagner et al.,[1] there has been a radical change in the management of adrenal masses because minimally invasive adrenalectomy has been shown to decrease the length of hospital stay, reduce health-care cost, reduce wound complications and blood loss and improve the patient's outcome with an earlier patient mobility and faster return to regular activity.[10] The literature defines the GAT adrenal masses larger than 6 cm.[3] GAT are considered rare, with an incidence ranging from 8.6% to 38.6% of all adrenal tumours.[4] The size criteria remain, at the moment, the subject discussed in literature for the main surgical approach. The size is an important variable in predicting malignancy, in fact, if the lesions are smaller than 4 cm, the risk of malignancy is approximately 2%, whereas for lesions of 4–6 cm, the risk of malignancy is 6%, and for lesions of 6 cm, the risk of malignancy is 25% (10%–53%).[5] At the moment, there are no evidence that suggest that a laparoscopic approach is contraindicated for GAT because the size is only a predictor factor of malignancy.[6],[11] Conversely, the open approach is recommended in patients with evidence at pre-operative imaging studies of malignancy with local invasion of adjacent structures, thus facilitating lymph node dissection and en bloc resection of adjacent structures to achieve negative margins.[12] An incomplete resection or capsular disruption increase the risk of local recurrence and intra-abdominal neoplastic dissemination.[13] It is mandatory to consider that surgeon experience, hospital volume and a multidisciplinary approach, which comprises surgeons, anaesthesiologists and endocrinologists, are three important parameters in the selection of such patients.[9]

Over the 10-year study, 50 (20.4%) out of 245 patients referred for adrenal tumours presented with GAT. Thirty-four of these patients (68%) were submitted to LA, 16 (32%) were submitted to OA. LA was technically safe and feasible. The surgical outcome of these patients, compared to OA patients, was better in terms of blood loss, hospital stay and operative time. No statistically differences were registered in terms of post-operative complication.

Laparoscopic adrenalectomies were performed using lateral transperitoneal approach. The lateral transabdominal approach is actually, the most widely practised since it provides a good exposure of the adrenal gland and surrounding structures and provides to surgeon precise anatomic landmark with a safe control to vascular structures. Moreover, it allows to treat other abdominal pathologies simultaneously.[14]

We have drawn up a set of technical caveats with 10 points to follow in all laparoscopic adrenalectomies, and in particular, for the treatment of GAT, based on laparoscopic adrenal surgery experience of our surgical centre [Table 3]. It is fundamental to mention the adequate position of the patient and the trocars to research the correct anatomic landmarks and the main adrenal vein; to avoid the breakdown of the adrenal capsule which would require conversion and to avoid the excessive manipulation of the tumour, in particular in presence of malignance GATs or pheochromocytomas moreover, GATs present a rich vascularisation, particularly observed in cases of pheochromocytoma and metastasis, and for this reasons, the use of clips and radiofrequency scalpel is mandatory. The anomalous adrenal vein anatomy has been described between 9% and 22%, in particular on the left adrenal gland.[15]
Table 3: The &10 points' to follow in all laparoscopic adrenalectomies

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Therefore, the LA offers significant advantages compared to open approach. The size of the tumour is not a contraindication to laparoscopy but is only a predictive factor of malignancy. Local ablative therapy is a safe and feasible in terms of surgical and oncological outcome if performed by an experienced laparoscopic surgeon and in high-volume centres. It is necessary to select the patients with GAT through an adequate pre-operative multidisciplinary study. The presence of radiological signs suggestive for malignancy such as vascular infiltration or of the adjacent organs is a contraindication to laparoscopy.


 ¤ Conclusion Top


LA offers significant advantages compared to open approach. The size of the tumour is not a contraindication to laparoscopy but is only a predictive factor of malignancy.

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patients have given their consent for their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

 
 ¤ References Top

1.
Gagner M, Lacroix A, Bolté E. Laparoscopic adrenalectomy in Cushing's syndrome and pheochromocytoma. N Engl J Med 1992;327:1033.  Back to cited text no. 1
    
2.
Lee JM, Kim MK, Ko SH, Koh JM, Kim BY, Kim SW, et al. Clinical guidelines for the management of adrenal incidentaloma. Endocrinol Metab (Seoul) 2017;32:200-18.  Back to cited text no. 2
    
3.
Zografos GN, Farfaras A, Vasiliadis G, Pappa T, Aggeli C, Vassilatou E, et al. Laparoscopic resection of large adrenal tumors. JSLS 2010;14:364-8.  Back to cited text no. 3
    
4.
Mege D, Taieb D, Lowery A, Loundou A, DE Micco C, Castinetti F, et al. Contemporary review of large adrenal tumors in a tertiary referral center. Anticancer Res 2014;34:2581-8.  Back to cited text no. 4
    
5.
NIH state-of-the-science statement on management of the clinically inapparent adrenal mass (”incidentaloma”). NIH Consens State Sci Statements 2002;19:1-25.  Back to cited text no. 5
    
6.
Lombardi CP, Raffaelli M, De Crea C, Boniardi M, De Toma G, Marzano LA, et al. Open versus endoscopic adrenalectomy in the treatment of localized (stage I/II) adrenocortical carcinoma: Results of a multiinstitutional Italian survey. Surgery 2012;152:1158-64.  Back to cited text no. 6
    
7.
Porpiglia F, Destefanis P, Fiori C, Giraudo G, Garrone C, Scarpa RM, et al. Does adrenal mass size really affect safety and effectiveness of laparoscopic adrenalectomy? Urology 2002;60:801-5.  Back to cited text no. 7
    
8.
Tanaka M, Ono Y, Matsuda T, Terachi T, Suzuki K, Baba S, et al. Guidelines for urological laparoscopic surgery. Int J Urol 2009;16:115-25.  Back to cited text no. 8
    
9.
Alemanno G, Bergamini C, Prosperi P, Valeri A. Adrenalectomy: Indications and options for treatment. Updates Surg 2017;69:119-25.  Back to cited text no. 9
    
10.
Heslin MJ, Winzeler AH, Weingarten JO, Diethelm AG, Urist MM, Bland KI. Laparoscopic adrenalectomy and splenectomy are safe and reduce hospital stay and charges. Am Surg 2003;69:377-81.  Back to cited text no. 10
    
11.
Parnaby CN, Chong PS, Chisholm L, Farrow J, Connell JM, O'Dwyer PJ. The role of laparoscopic adrenalectomy for adrenal tumours of 6 cm or greater. Surg Endosc 2008;22:617-21.  Back to cited text no. 11
    
12.
Henry JF, Sebag F, Iacobone M, Mirallie E. Results of laparoscopic adrenalectomy for large and potentially malignant tumors. World J Surg 2002;26:1043-7.  Back to cited text no. 12
    
13.
Tsuru N, Suzuki K, Ushiyama T, Ozono S. Laparoscopic adrenalectomy for large adrenal tumors. J Endourol 2005;19:537-40.  Back to cited text no. 13
    
14.
Gumbs AA, Gagner M. Laparoscopic adrenalectomy. Best Pract Res Clin Endocrinol Metab 2006;20:483-99.  Back to cited text no. 14
    
15.
Ford KM, Smolinski S, Perez Lozada JC. Anomalous adrenal vein anatomy complicating the evaluation of primary hyperaldosteronism. Radiol Case Rep 2018;13:139-41.  Back to cited text no. 15
    


    Figures

  [Figure 1]
 
 
    Tables

  [Table 1], [Table 2], [Table 3]



 

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