Retroperitoneal tumor finally diagnosed as a bronchogenic cyst: A case report an

Yang-Yang Gong, Xin Qian, Bo Liang, Ming-Dong Jiang, Jun Liu, Xing Tao, Jing Luo, Hong-Jian Liu,You-Gang Feng

Abstract

Key Words: Adrenal gland neoplasm; Bronchogenic cyst; Retroperitoneal; Subdiaphragmatic; Pancreatic cyst; Case report

lNTRODUCTlON

Retroperitoneal bronchogenic cysts (RBCs) are rare retroperitoneal tumors. Most bronchogenic cysts occur in the thoracic cavity but are rare occurrences in the retroperitoneum. They consist of respiratory epithelium, smooth muscle, cartilage, and mixed serous and mucous glands. The cysts are filled with high-viscosity, protein-rich mucus. Patients usually have no symptoms or have only mild abdominal pain. Most RBCs are found incidentally during an examination for another disease. Bronchogenic cysts originate in the foregut, form at about 3-7 wk of embryonic development, and are usually benign. Milleret al[1] reported the first case of a RBC in 1953. With increasing attention to health and awareness of the value of physical examination, more and more RBCs have been found, especially in patients in developing countries. However, most clinicians even in developed areas are not familiar with RBC. We used the keywords "bronchogenic cyst AND (adrenal OR retroperitoneal OR subdiaphragmatic)" to search for related articles in PubMed. Only 80 articles have been published to date, including 4 that could not be obtained as full-text publications.

CASE PRESENTATlON

Chief complaints

A tumor was found in the left retroperitoneum during a routine follow-up examination.

History of present illness

The patient reported having no feelings of discomfort prior to entering our hospital, nor any weight loss or cachexia caused by the inability to eat.

History of past illness

The patient had a history of brain surgery for a ruptured intracranial aneurysm 6 mo previously. She had no other relevant medical history other than a 6-year history of hypertension that was controlled by amlodipine besylate tablets.

Personal and family history

The patient revealed that there was no special personal and family history.

Physical examination

The patient's body temperature was 36.6 °C, and she reported having no fever for more than 1 mo before presentation. Her blood pressure was 124/86 mmHg, and there was no shortness of breath. There was no percussion pain in the costovertebral angle on either side, and no abdominal tenderness, rebound pain, nor other positive signs.

Laboratory examinations

Routine blood examination did not find any obvious abnormal results other than a slightly low plasma albumin level.

Imaging examinations

Contrast-enhanced computed tomography (CT) revealed an oval, 54 mm × 40 mm cystic, moderatedensity mass near the left adrenal gland. It showed a clear boundary and a uniform density of 85 HU (Figure 1).

Further diagnostic workup

The patient’s findings for 24-h urine, 17 ketones, 17 hydroxyls, adrenocortical hormone, serum potassium concentration, serum amylase, lipase, and epithelial tumor markers, as well as endocrinological results were normal.

FlNAL DlAGNOSlS

RBC.

TREATMENT

As we were not sure whether the tumor was benign or malignant, and to avoid the possibility of a malignant tumor and further growth, we performed a retroperitoneal laparoscopic exploration. With the patient placed in the right oblique position, laparoscopy found a mass of about 54 mm × 40 mm with a cystic appearance. The base was located in the upper part of the medial branch of the left adrenal gland, behind the pancreas. It adhered to the pancreas and surrounding tissues. The cyst ruptured unexpectedly in the process of being dissociated and it released some of its contents, which appeared as a brown jelly-like substance (Figure 2). We immediately applied negative pressure drainage to suck out the contents of the cyst to prevent spreading. After the cyst was completely removed, we examined the surrounding adjacent tissue and found no obvious changes. Postoperative pathological examination showed respiratory epithelium, smooth muscle, cartilage, and mucous glands (Figure 3), consistent with an RBC.

OUTCOME AND FOLLOW-UP

The patient was discharged from the hospital on the 4thday after operation. After follow-up of more than 6 mo, the tumor did not recur and the patient did not have any tumor-related symptoms. The patient did not receive further treatment.

DlSCUSSlON

Origin

RBCs arise from abnormal development of the foregut in the early stage of embryonic development. Sumiyoshiet al[2], Swansonet al[3], and Reicheltet al[4] described the connection of the abdominal cavity and thoracic cavity by pericardial ducts at about 3-7 wk of gestation, and the development of the ventral or dorsal part of the foregut developed into the tracheobronchial tree and esophagus. Bronchogenic cysts usually occur in the lungs or the posterior mediastinum[5,6]. With the formation of the diaphragm, some dysplastic tracheobronchial trees may be cut off, forming ectopic bronchogenic cysts under the diaphragm[7,8]. Another hypothesis is that RBCs originate from abnormal differentiation of abdominal foregut-derived cysts[9]. Pluripotent differentiated primordial cells from the ventral foregut migrate to the abdomen, where they differentiate into bronchogenic cysts containing cartilage or esophageal and gastrointestinal cysts with different characteristics[10].

Clinical features

The prevalence of bronchogenic cysts in the general population is estimated to range from 1/42000 to 1/68000[11]. It is higher in men than in women, with a male:female ratio of 4:1[12]. About 86% of bronchogenic cysts occur in the mediastinum and lungs[13]. RBCs are very rare, accounting for only 0.03% of all cases[5]. Our search of the published literature found a total of 80 articles published in English. A total of 86 cases were described (48% in men and 52% in women). The age at diagnosis ranged from prenatal to 75 years[14-17]. The average age at diagnosis was 39 ± 16 years and 82% were diagnosed in patients between 20 years and 60 years of age.

Figure 1 Abdominal enhanced computed tomography image. A: Transverse section; B: Coronal section. The mass was located around the left adrenal gland. The 54 mm × 40 mm oval mass showed a clear boundary and a uniform density of 85 HU.

Figure 2 Photograph of the surgical procedure. Cyst fluid was visible during the retroperitoneal laparoscopy, showing a brown semiliquid consistency that was rich in protein.

Figure 3 Histopathological examination of the cyst wall. A: Pseudostratified ciliated columnar epithelium, cilia and smooth muscle (hematoxylin and eosin, 200 ×); B: Pseudostratified ciliated columnar epithelium, hyaline cartilage and bronchial glands (hematoxylin and eosin, 100 ×).

Most RBCs described in the literature appeared to the left of the midline, accounting for almost 78% of cases. This is similar to the 82% reported by Lianget al[18] that were found within a triangle behind the stomach, defined by the midline, splenic vein, spleen, and diaphragm. Given the location, it is possible that during embryonic development, the caudal primitive foregut is related to the counterclockwise transposition of the midgut from left to right, while the exfoliated germ remains on the left side[19]. In addition, in the 3rdweek of embryonic development, the development of the liver hinders abnormal sprouting of the tracheobronchial tree, and it enters the diaphragm[20]. About 73% of the bronchogenic cysts on the left are near the left adrenal gland. Bronchogenic cysts near the right adrenal gland accounted for about 12% of the reports. There is only one reported case of a bilateral bronchogenic cyst surrounding both adrenal glands[21] and two cases on the inferior midline of the diaphragm or in front of the abdominal aorta[22,23]. Bronchogenic cysts located around the pancreas account for about 10% of the reported cases, and an interesting case occurred in the left iliac fossa[24]. The average diameter of the RBCs in published reports was 5.8 cm, with a maximum diameter of about 20 cm in a case reported by Mirsadeghiet al[25]. We did not find a correlation of tumor size with age.

Bronchogenic cysts are usually not symptomatic unless they are accompanied by a secondary infection, perforation, bleeding, or compression of the adjacent organs[26]. Bronchogenic cysts that occur in the chest may be accompanied by retrosternal pain, dysphagia, cough, fever, and hemoptysis[16]. RBCs are located close to the adrenal glands, kidney, pancreas, or gastrointestinal tract, and may be accompanied by upper abdominal pain, digestive tract symptoms (nausea, vomiting), and back pain.

In our review of the 86 previously reported RBCs, about 48% were not symptomatic, and were incidental finding during a physical examination conducted for an unrelated reason. About 46% were accompanied by waist or abdominal pain or discomfort that was most likely caused by increased cyst volume and compression of adjacent organs, which is different from the percentage reported by Lianget al[18]. Six cases were accompanied by digestive tract symptoms, five by back pain, four by varying degrees of weight loss, and one by a secondary infection associated with the cyst[27]. One case was accompanied by a urinary tract infection, but it was not clear whether the infection was associated with the cyst[7]. Doggettet al[28] reported pheochromocytoma-like symptoms in a 44-year-old patient with cyst compression of the adrenal gland, but our review found that RBCs rarely caused adrenal hypofunction, Cushing syndrome, or pheochromocytoma. Most patients with a history of hypertension had no significant decrease in their blood pressure after relief of the compression.

Imaging examination

It is often difficult to diagnose RBCs by imaging examinations. Ultrasonography is not useful, especially if the fluid density within the cyst is high. In most cases, CT and magnetic resonance imaging (MRI) are more useful. In our case, CT showed a nearly round, well-defined, low-density homogeneous mass with no significant enhancement after injection of contrast medium (Figure 1). Most RBCs are unilocular, but irregularly shaped septal cysts have been reported[25,29]. The fluid within RBCs is usually rich in protein and mucus, and they produce a low-density shadow on CT. The cyst density has been reported to range from 6-100 HU, varying with the protein content[6,17]. The CT performance varies according to differences in the other components of the fluid in the capsule. Bleeding, infection, or calcification in the cyst are seen as a high-density shadow with uneven density[19,30-32], and increased bleeding or a highprotein content make it easy to mistake the RBC for a solid or cystic solid tumor[30,33].

MRI is more valuable in the diagnosis of RBCs. Cysts with serous fluids and a low protein concentration have a low signal intensity on T1-weighted images and enhanced signal intensity on T2-weighted images[13,34,35], but most RBCs contain a thick protein solution and have high signal intensity on both T1- and T2-weighted images[31]. In addition, fat-suppressed T1-weighted images can be used to distinguish bronchogenic cysts from malignant masses like teratomas and dermoid cysts[36-38]. Duanet al[39] and Fiorelliet al[40] have shown that Technetium (99mTc)-methoxyisobutylisonitrile (commonly known as MIBI) is involved in the transport of P-glycoprotein and that P-protein is highly expressed in malignant tumors; consequently, 99mTc-MIBI-single-photon emission computed tomography (commonly known as SPECT) can be used to differentiate benign from malignant tumors. Yoonet al[41] and Brientet al[42] found that RBCs have no fluorodeoxyglucose uptake, which can be used to evaluate the degree of infection or the malignant changes of RBCs.

Differential diagnosis

As RBCs do not have specific clinical characteristics, none of the previously reported cases have been accurately diagnosed before surgery or an invasive procedure. A preoperative differential diagnosis would help clinicians to choose the most appropriate treatment. About 73% of RBCs are found around the left adrenal gland, and adrenal tumors are usually considered as the initial diagnosis. If the mass is located around the adrenal gland, then serum potassium, 24-h urinary cortisol, cortisol, and basal serum adrenocorticotropic hormone levels can exclude Cushing syndrome. Urinary catecholamine and plasma norepinephrine can detect the presence of a pheochromocytoma[34]. If the lesion is located around the pancreas, serum amylase and lipase levels must be determined. Cassianiet al[43] reported elevated serum amylase (119 U/L) in a patient with endoscopic ultrasound guided fine-needle biopsy. That patient was eventually diagnosed with an RBC, but RBCs usually do not cause an increase in serum amylase. Except for 1 case with serum carbohydrate antigen (CA)19-9 and carcinoembryonic antigen (CEA) levels higher than 1200 U/mL[1], no significant increase of tumor markers has been reported. We believe that the levels of tumor markers such as CA19-9, β-human chorionic gonadotropin, afetoprotein, and CEA are of value in determining whether retroperitoneal masses are malignant.

Jannaschet al[44] described the histology of 15 cases of RBCs, which included involvement of respiratory epithelium (100%), hyaline cartilage (73%), smooth muscle (80%), and serous or bronchogenic glands (93%), and without immature components, atypia, or tumor necrosis. Microscopically, the inner surface of RBCs is pseudostratified ciliated columnar epithelium, with a small number of goblet cells. The cyst wall is comprised of dense fibrous connective tissue with lymphatic plasma cell infiltration and partial calcification[45]. Other components include tiny arteries, veins, capillaries, nerves, and rare smooth muscle fibers[28]. Our case had histological features characteristic of bronchogenic cysts, including respiratory epithelium, smooth muscle, cartilage, and mucous glands. Most often, the fluid within the RBC capsule is thick mucus, rich in protein. Calcium deposits have been reported[46,47] but are very rare.

Table 1 Tumor size of retroperitoneal bronchogenic cysts

The majority of retroperitoneal tumors are malignant[48], and although there are cases of malignant transformation of RBCs[49], they are generally benign. In addition to RBCs, other retroperitoneal benign tumors include fibromatosis, lipomas, angiolipomas, and leiomyomas. The differential diagnosis should include cystic teratoma, bronchopulmonary sequestration, cystic lymphangioma, mucinous cystadenoma, cystic mesothelioma, Müllerian cyst, epidermoid cyst, tail cyst, solid tumor cystic degeneration, retroperitoneal pseudomyxoma, and other retroperitoneal neoplastic lesions. Nonneoplastic lesions include pancreatic pseudocyst, non-pancreatic pseudocyst, lymphoid cyst, urinoma, and hematoma.

In addition to adrenocortical or medullary tumors, RBCs should be differentiated from cystic teratoma, bronchopulmonary sequestration, and esophageal cysts. Mature cystic teratoma often occurs in the midline[50] and most bronchogenic cysts are located to the left of the midline. If there is low attenuated fat in the cyst and calcification of the cyst wall on CT, then cystic teratoma is more likely[33]. Cystic teratomas include bronchogenic tissue derived from endoderm and other tissues derived from mesoderm and ectoderm. RBCs do not have those structures[29]. Bronchopulmonary sequestration consists of differentiated lung parenchyma, bronchus, and pleural tissue[8,50] that can be easily differentiated from RBCs. Esophageal cysts have two layers of smooth muscle, often with squamous epithelium and no cartilage[8,29].

Treatment

Preoperative diagnosis of RBC is difficult. Before obtaining pathological or histological results, if malignant tumors cannot be excluded, surgical treatment is recommended to make a clear diagnosis, relieve symptoms, and prevent complications. Retroperitoneal laparoscopic surgery[51], laparoscopic surgery[52], and open surgery[16] have been proven to be safe and effective. There is no evidence that either transabdominal or retroperitoneal approaches are more advantageous[44]. Retroperitoneal approaches may reduce pain, but the choice of surgical methods or approaches should be based on the clinician's preference. If the patient's physical condition permits, the preoperative diagnosis can be completed by fine-needle aspiration[16,53]. If the biopsy results are consistent with bronchogenic cysts, conservative treatment is also feasible if the patient is asymptomatic and the cyst has a small diameter.

We found that the diameter of cysts in reports of patients with lumbar and abdominal pain was 6 cm, while the diameter of cysts in patients without pain was 4 cm (Table 1). Although fine-needle aspiration biopsy is considered safe, it can lead to malignant cell spread and false-negative results[54]. When patients choose conservative treatment, they must be informed that their symptoms may worsen as the diameter of the tumor increases, although the increase is generally very slow. Brientet al[42] reported a patient diagnosed with an RBC without surgical treatment who remained stable after 3 years of followup.

CONCLUSlON

RBCs are a benign developmental abnormality with the possibility of malignant transformation. At least half of the patients have no obvious symptoms. If present, the typical clinical symptoms are abdominal pain and gastrointestinal reactions. Endocrinological examination is usually not specific, and MRI is superior to CT. Typical histological findings include respiratory epithelium, smooth muscle, cartilage, and mucous glands. Fine-needle biopsy can be helpful for a definite diagnosis. Conservative treatment is feasible for selected patients. We recommend that RBCs with no symptoms and less than 4 cm in size be treated conservatively. Symptomatic cysts larger than 4 cm can be treated by surgery, and those larger than 6 cm should be surgically removed regardless of whether the patient has symptoms or not. Three surgical methods — retroperitoneal laparoscopic surgery, laparoscopic surgery, and open surgery — have been used successfully.

ACKNOWLEDGEMENTS

The authors thank Dr. Cai X and Dr. Ran C for their assistance with literature searching and checking of the results.

FOOTNOTES

Author contributions:Gong YY collected the case data, obtained the clinical data, drafted and revised the manuscript, and was a major contributor in writing the manuscript; Qian X acquired all the published articles from the literature database and performed the data extraction; Jiang MD and Liu HJ analyzed the clinical data; Liang B and Liu J was responsible for revising and editing of the manuscript for important intellectual content; Tao X and Luo J edited the figures and tables; Feng YG advised on all stages of the study; all authors read and approved the final manuscript.

lnformed consent statement:Written informed consent was obtained from the patient for the publication of this case report and the accompanying images.

Conflict-of-interest statement:The authors declare that they have no competing interests.

CARE Checklist (2016) statement:The authors have read the CARE Checklist (2016), and the manuscript was prepared and revised according to the CARE Checklist (2016).

Open-Access:This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BYNC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is noncommercial. See: https://creativecommons.org/Licenses/by-nc/4.0/

Country/Territory of origin:China

ORClD number:Yang-Yang Gong 0000-0001-7219-747X; Xin Qian 0000-0002-3577-2946; Bo Liang 0000-0002-0486-0804; Ming-Dong Jiang 0000-0001-8918-2987; Jun Liu 0000-0001-9481-5881; Xing Tao 0000-0003-2163-7898; Jing Luo 0000-0001-8149-998X; Hong-Jian Liu 0000-0002-9605-9570; You-Gang Feng 0000-0003-3577-5773.

S-Editor:Yan JP

L-Editor:A

P-Editor:Yan JP