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Oncology Letters logoLink to Oncology Letters
. 2018 Feb 2;15(4):5318–5324. doi: 10.3892/ol.2018.7925

Multi-institutional survey of carotid body tumors in Japan

Aya Ikeda 1, Kiyoto Shiga 1,, Katsunori Katagiri 1, Daisuke Saito 1, Jun Miyaguchi 1, Shin-Ichi Oikawa 1, Kodai Tsuchida 1, Takahiro Asakage 2, Hiroyuki Ozawa 3, Ken-Ichi Nibu 4, Naoki Ohtsuki 4, Yasushi Fujimoto 5, Ken-Ichi Kaneko 6
PMCID: PMC5840754  PMID: 29552173

Abstract

There has been no attempt to clarify the status of patients with carotid body tumor (CBT) in Japan. This multi-institutional survey analyzed patients with CBT throughout Japan by gathering information on these patients from institutions that performed head and neck surgeries. Information from a total of 150 patients from 25 institutions from the past 20 years was employed in the present survey. There were 87 females and 63 males, and their mean age was 48.0 years old. The most common chief complaint was a neck mass and the mean suffering period was 46.1 months. Eighteen patients had a family history of paragangliomas and fifteen patients had bilateral CBTs. Among the 94 patients who underwent surgery to remove a CBT, 23 patients had tumors classified as Shamblin type I, 59 had type II and 12 had type III. The most frequent feeding artery of these CBTs was the ascending pharyngeal artery. Preoperative embolization of these arteries was effective in reducing blood loss; however, the operation time in Shamblin type I and II tumors was not improved. Thus these results revealed the status of patients with CBT and their treatment throughout Japan.

Keywords: carotid body tumor, Japan, multi-institutional survey, family history, paraganglioma, surgery, blood loss and operation time, preoperative embolization of the feeding artery

Introduction

Carotid body tumor (CBT) is a rare disease derived from carotid body paraganglion cells. The characteristic feature of this tumor is a rich vascular network in its contents and capsules supplied by many feeding arteries (1). As the risk of complications such as cranial nerve paralysis increases as the tumor grows, surgical resection is recommended for all CBTs in otherwise healthy patients (2,3). Moreover, there is a small but definite risk of malignancies for all paragangliomas (47). Molecular biological study has so far revealed that this tumor has various types of gene alterations such as point mutations in the SDH gene family (2,8,9). A total of 10 to 35% of patients with CBT are estimated to harbor a hereditary predisposition and SDHD is the most common mutation, followed by SDHB and then SDHC (2). In one review, it was reported that SDH germ-line mutations are present in 31% of patients with head and neck paragangliomas (10). The concept of the ‘hereditary paraganglioma-pheochromocytoma syndrome’ has arisen to describe familial paraganglioma patients, which includes CBT patients with a family history and gene alterations (1113).

The low incidence rate of this tumor and absence of a registration and study system has prevented detailed research to be performed to clarify the present status of this tumor in Japan. Also the status of SDHx gene mutations was not obvious because of genetic testing was not performed for these patients. We organized a study group, which we call the Japan Carotid Body Tumor Research Group (JCBTRG), and initiated a survey of the patients with CBT in Japan. The goal of our study is to reveal the overall aspects of gene alteration patterns, such as those present in the SDH gene family, among patients in Japan. Initially, we began with a survey of the status of patients throughout Japan. Here we report the characteristic features of CBT patients in Japan unveiled from our studies.

Patients and methods

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2008.

The study design was a multi-institutional retrospective review of medical records. Research protocols were assessed and accepted by the institutional research boards of individual institutions.

We sent the research format for cases of CBT to 635 authorized institutions that had specialists who were members of the Japan Otolaryngology Society. A total of 316 responses were sent back to the research bureau at Iwate Medical University and 150 patients were registered from 25 institutions in our study. There were 204 hospitals or institutions that did not have CBT patients for 20 years. Information on the CBT patients was summarized and analyzed. The analyzed items were gender, age, family history, size, Shamblin classification (Fig. 1) (1), location of the patients, operation time of extirpation surgery, amount of blood loss, preoperative embolization of the feeding arteries and resection and repair of the carotid arteries. Statistical analyses were carried out using Students' t-test.

Figure 1.

Figure 1.

Shamblin classification. Typical appearance of Shamblin type I, II and III tumors are shown and their association with carotid arteries has been indicated. Type I tumors are localized within the carotid arteries. Type II tumors partially adhere to or surround the carotid arteries. Type III tumors completely surround at least one of the carotid arteries. ICA, internal carotid artery; ECA, external carotid artery.

Results

From 1995 to 2015, 399 patients with CBT were referred to 112 institutions. In summary, 194 patients underwent surgery and 205 patients were under follow-up without surgery. Patients with CBT from these institutions were registered in our study and we obtained 150 summarized patient records from 25 institutions. There were 87 females and 63 males and their mean and median age were 48.0 years old and 49 years old, respectively, ranging from 8 to 78 years old (Fig. 2). Fifty to 60 year old patients were the most dominant throughout all age groups followed by 40 to 50 year old patients. There was an 8 year old patient as well. As for gender, female patients were dominant in almost every age group. Fifteen patients had bilateral CBTs resulting in 165 CBTs.

Figure 2.

Figure 2.

Age and gender distribution of patients with carotid body tumors in Japan. The mean and median age of the patients were 48.0 and 49 years old, respectively.

The chief complaints of the patients with CBT are shown in Table I. Neck tumors were the most frequent chief complaint in these patients and 125 patients (83.3%) complained of neck tumors. The second chief complaint was an incidental recognition of the tumor by some modalities such as CT scan or MRI (14 patients, 9.3%). There were some patients who complained of hoarseness (3 patients, 2.0%), pharyngeal discomfort (2 patients, 1.3%) dysphagia, hearing loss, numbness of the body, or chest discomfort. Four patients (2.7%) complained of pain. The mean and median suffering period was 46.1 months and 10.5 months, respectively, ranging from 0 months to 480 months.

Table I.

Chief complaint in the 150 patients with carotid body tumors.

Complaint type Number of the patients Percentage of total patients (%)
Neck tumor 125 83.3
Incidental recognition 14 9.3
Pain 4 2.7
Hoarseness 3 2.0
Pharyngeal discomfort 1 0.6
Dysphagia 1 0.6
Hearing loss 1 0.6
Numbness of the body 1 0.6
Chest discomfort 1 0.6

Eighteen patients had a family history of paragangliomas (Table II). There were 10 male and 8 female patients. Five patients had fathers who had a type of paraganglioma; namely, CBT, vagal paraganglioma, or pheochromocytoma (Cases 1, 3, 5, 6 and 12) and the other 4 patients had a father who was expected to have a type of paraganglioma (Cases 2, 10, 14 and 17). Two patients had a brother and a sister with paragangliomas and two patients had a brother and a sister who were assumed to have paragangliomas. A patient had sons with paragangliomas and two patients had a daughter with CBT. Two patients had bilateral CBTs.

Table II.

Family history of patients with CBT.

Case no. Age (years) Gender Family members Comments
  1 30 Male Father: CBT+vagal paraganglioma Aunt: CBT
  2 23 Female Father: Renal tumor (pheochromocytoma?)
  3 40 Female Father: Pheochromocytoma elder brother: Pheochromocytoma
  4 56 Female Younger brother: Vagal paraganglioma
  5 40 Male Father: CBT elder brother: CBT
  6 45 Male Father: CBT younger brother: CBT Bilateral CBTs
  7 72 Male Sons: CBT
  8 49 Male Daughter: CBT
  9 53 Male Elder sister: Glomus tumor paternal cousin: Glomus tumor
10 48 Female Father: Bilateral tumor of the neck(CBT?)
11 37 Male Details unknown
12 29 Female Father: CBT
13 56 Male Daughter: CBT
14 51 Male Father: Details unknown
15 59 Male Younger sister: Details unknown Bilateral CBTs
16 58 Female Elder brother: Details unknown
17 42 Female Father: Details unknown
18 19 Female Grandmother: Details unknown

Cases 5, 6 and 7 were relatives, and cases 12 and 13 were relatives. CBT, carotid body tumor.

Seven patients had metastases that included the lymph nodes in 5 patients and the lung in 3 patients. As for other paragangliomas, 4 patients had pheochromocytomas, two of which were malignant. Two of these patients had a family history. Three patients had glomus tumors and 2 patients had mediastinal paragangliomas. One patient had von Hippel Lindau disease.

Although the survey covered all prefectures, there were some tendencies that indicated the frequency of CBT was dependent on the area where the patients lived or the hospitals to which they were referred. Table III shows the frequencies of CBT patients according to the institutions to which they were referred. There were 28 prefectures that had no patient with CBT registered in our study. The other 19 prefectures had more than one patient registered to our study. One-third of the patients (57 patients) were located in the Tokyo area where medical institutions were gathered. Fifteen patients were registered from Aichi and Hyogo. Eleven and ten patients were from Iwate and Miyagi, respectively. Nine patients were from Hokkaido and Nagasaki, respectively.

Table III.

Location of patients with carotid body tumors in Japan.

Prefecture Male Female Total
Hokkaido 4 5 9
Iwate 3 8 11
Miyagi 5 5 10
Fukushima 0 1 1
Saitama 0 3 3
Chiba 0 1 1
Tokyo 20 37 57
Kanagawa 2 0 2
Niigata 2 2 4
Fukui 1 0 1
Aichi 6 9 15
Mie 1 2 3
Hyougo 7 8 15
Nara 0 2 2
Hiroshima 0 2 2
Fukuoka 1 0 1
Nagasaki 7 2 9
Kumamoto 2 0 2
Okinawa 2 0 2
Total no. of patients 63 87 150

Ninety-four patients underwent surgery and 6 patients underwent radiation therapy. The other patients remained under observation because of the patients' choice or physicians' recommendation. The treatment choice of these patients depended on the institutions to which they were referred.

Among the 94 patients including 4 patients with bilateral CBTs who underwent surgery to remove a CBT, 23 patients had tumors classified as Shamblin type I, 59 had type II and 12 had type III (Table IV). Classification of tumors from four patients were not recorded nor undone. The feeding arteries of 76 tumors were preoperatively embolized before resection of the CBT (Table IV). The average tumor size in diameter was 26.3 mm in Shamblin type I tumors, 37.3 mm in type II tumors and 36.7 mm in type III tumors.

Table IV.

Shamblin classification.

A, Size in diameter (mm)

Shamblin classification

Variable I II III Average
Mean 26.3 37.3 36.7 34.6
Median 24.5 38.0 35.5 35.0

B, Preoperative embolization (n)

Shamblin classification

Variable I II III Total

+ 19 48   9 76
  4 11   3 18
Total (n) 23 59 12 94

A total of 94 patients, including 4 patients with bilateral carotid body tumors, underwent surgery. Classification of the tumors from 4 patients were not recorded/performed.

We analyzed the relationship between operation time of the surgery and the amount of blood loss. Fig. 3 shows the result of the analysis. The calculated coefficient correlation was 0.69 for all patients. According to Shamblin classification, mean operation time of the surgery and the mean amount of blood loss were 229 min and 77.8 ml in Shamblin I, 262 min and 229 ml in Shamblin II, 461 min and 404 ml in Shamblin III, respectively. As for operation time, there were significant differences between Shamblin I and II (P=0.016) and Shamblin I and III (P<0.001) (Table V). While as for the amount of blood loss, there were significant differences between Shamblin I and III (P<0.001) and Shamblin II and III (P<0.001) (Table V).

Figure 3.

Figure 3.

Distribution of blood loss and operation duration of surgery for carotid body tumors. Shamblin type I, II and III tumors are indicated by open circles, gray circles and closed circles, respectively. The x-axis indicates the operation time (min) and the y-axis indicates the amount of blood loss (ml).

Table V.

Blood loss and operation time by Shamblin classification.

Variable Shamblin I Shamblin II Shamblin III P-value
Mean blood loss (ml) 78 229 404   I vs. II: 0.016
II vs. III: 0.082
I vs. III: <0.001
Mean operation time (min) 229 262 461 I vs. II: 0.40
II vs. III: <0.001
I vs. III: <0.001

Table VI shows the main feeding arteries of 78 tumors detected by carotid arteriography. Most frequent feeding artery was the ascending pharyngeal artery followed by the superior thyroid artery and the occipital artery. It is noteworthy that in some patients, feeding artery was derived from external carotid artery (n=7) and internal carotid artery (n=1).

Table VI.

Main feeding arteries of carotid body tumors.

Feeding artery Number of the patients (%)
Ascending pharyngeal artery 50 (64.1)
Superior thyroid artery 18 (23.1)
Occipital artery 17 (21.8)
External carotid artery 7 (9.0)
Lingual artery 6 (7.7)
Posterior auricular artery 4 (5.1)
Facial artery 2 (2.6)
Ascending palatine artery 2 (2.6)
Superficial temporal artery 1 (1.3)
Common carotid artery 1 (1.3)
Internal carotid artery 1 (1.3)

Cases that included multiple main feeding arteries have also been indicated in this table.

When the patients underwent preoperative embolization, mean operation time of the surgery and the mean amount of blood loss were 240 min and 55.9 ml in Shamblin I, 255 min and 178 ml in Shamblin II, 468 min and 406 ml in Shamblin III, respectively. While the patients did not undergo preoperative embolization, mean operation time of the surgery and the mean amount of blood loss were 181 min and 171 ml in Shamblin I, 290 min and 468 ml in Shamblin II, 440 min and 396 ml in Shamblin III, respectively. As for the amount of blood loss, there was a significant difference between the patients with preoperative embolization and those without that in Shamblin I and II tumors (Table VII, P=0.038 and P=0.0011, respectively).

Table VII.

Operation time and blood loss during surgery with or without preoperative embolization.

A, Operation time

Shamblin classification Total time (min) Embolization (−) Embolization (+) P-value
I 229±97 240±102 181±38 0.317
II 262±138 255±123 290±183 0.496
III 461±115 468±104 440±139 0.524

B, Blood loss during surgery

Shamblin classification Total quantity (ml) Embolization (−) Embolization (+) P-value

I 78±114 56±45 171±226 0.038
II 229±271 178±206 468±387 0.0011
III 404±203 406±218 396±147 0.623

Data are presented as the mean ± standard deviation.

Patients with Shamblin I tumor underwent no resection of carotid artery. Twenty-one out of 59 patients with Shamblin II tumor underwent resection of external carotid artery (ECA) and 2 patients underwent reconstruction of internal carotid artery (ICA), while all 12 patients with Shamblin III tumor underwent resection of ECA and 10 patients underwent reconstruction of ICA (Table VIII).

Table VIII.

Damage and repair to the carotid arteries.

Variable Shamblin I Shamblin II Shamblin III Total
Number of patients 23 59 12 94
Resection of ECA   0 21 12 33 (33.7%)
Reconstruction of   0   2 10 12 (12.2%)
ICA

Four tumors were not classified and were omitted from this table. ECA, external carotid artery; ICA, internal carotid artery.

Fifty-five (56%) patients who underwent surgery exhibited some postoperative complications (Table IX). The most frequent complication was vagal nerve paralysis, including recurrent nerve palsy in 22 (23%) patients, followed by hypoglossal nerve paralysis in 18 (19%). Thirteen patients exhibited two or more nerve paralysis episodes; the most frequent combination was that of vagal and hypoglossal nerve paralysis. Most of these complications were transient, but a patient underwent phonosurgery afterwards. There was no mortality in this cohort of patients after surgery.

Table IX.

Postoperative complications following carotid body tumor surgery.

Postoperative complication Total number Embolization (−) Embolization (+)
X paralysis 22 4 18
XII paralysis 18 5 13
First bite syndrome 10 0 10
Horner syndrome   7 0   7
IX paralysis   6 1   5
VII marginal branch paralysis   4 0   4
Dysphagia   4 0   4
XI paralysis   1 0   1
Hypertension   1 1   0
Orthostatic hypotension   1 0   1
Tunnel vision   1 1   0
Vertigo   1 0   1
Carotid artery stenosis   1 0   1
Cerebral infarction   1 1   0
Total no. of cases 55 out of 94 patients 9 out of 18 patients 46 out of 76 patients

There was no significant difference in the prevalence of these complications between the 2 groups of patients.

Discussion

As it is well known that CBTs are very rare, detailed features of this tumor have not been clarified in Japan. One of the reasons is that there has been no registration and study system until we organized the study group JCBTRG and initiated the survey of patients with CBT. By recruiting CBT patients to our survey from 635 authorized institutions for specialists of the Japan Otolaryngology Society, we could include CBT patients from throughout Japan as a whole even if some of the patients were not registered in our research system.

In accordance with our expectations, the number of female CBT patients was more than that of male patients. Although Shamblin's reports showed that the number of male patients was twice as many as that of female patients (1), most reports have shown that the number of female patients was more than that of male patients (3,1316).

The most common chief complaint in our patients was neck tumors and 83.3% of the patients complained of a neck tumor. As expected, their suffering periods were relatively long compared to those of other neck tumors, especially malignant ones. The longest suffering period was 40 years, indicating CBT has a characteristic feature of being a slow growing neck mass because most CBTs are benign. As some patients showed paralysis of the vagal nerve, which led to symptoms such as hoarseness and dysphagia, physicians must treat CBT neck tumors when they recognize vagal nerve paralysis as a differential diagnosis.

Eighteen patients (12%) had a family history of some kind of paraganglioma. This frequency was compatible with previous reports (12,17,18). Perhaps on-going analysis of gene mutations and clarification of gene mutation status could lead to recognition of more family members in Japanese CBT patients. In fact, a father and a daughter from Miyagi prefecture had the same mutation in the SDHD gene (18). Similar results were reported from Korea and China (19,20).

Seven patients (4.7%) had metastases of CBT and their tumor was diagnosed as a malignant CBT. This frequency was compatible with previous reports (47,21). It is well known that, as histopathological examination cannot distinguish a malignant tumor by morphological features in microscopic findings, malignancy or not is diagnosed by metastatic activity, namely clinical findings. The necessity of surgical resection depends on this aspect of tumor malignancy if it is not frequent. Head and neck surgeons must consider surgical resection of CBT once a patient is referred to our hospital.

The uneven distribution of the CBT patients is perhaps reflected in the uneven distribution of the population and medical institutions in Japan. Tokyo is the capital city of Japan and her population is over 10,000,000. However, as Japan has a population of approximately 120,000,000, it is not reasonable to expect that one-third of the CBT patients would be from the Tokyo area. Maybe the number of medical institutions also influenced the majority of patients being from the Tokyo area. Although Aichi and Hyogo have reasonable population sizes for the number of CBT patients, Iwate, Miyagi and Nagasaki have smaller populations, which were not reasonable for the number of their CBT patients. As we previously reported (18), CBT patients in Miyagi and Iwate (next to Miyagi) have the possibility of having the same gene alterations. These results indicated the possibility that some gene alterations penetrated into other areas in Japan such as Miyagi, Iwate and Nagasaki. Further investigation is needed to clarify the gene alterations of CBT patients in these high incidence areas.

As the characteristic feature of this tumor is a rich vascular network in its contents and capsules supplied by many feeding arteries, surgeons must be extremely careful to resect CBT because careless procedures result in vessel damage and much blood loss, especially damage of carotid artery lead to reconstruction of it. Preoperative angiography revealed that the most frequent feeding artery was the ascending pharyngeal artery followed by the occipital artery and the superior thyroid artery. Our result indicated that the direct feeding arteries derived from external carotid artery were relatively common, if not so many, in CBT patients (9%, 7 out of 78 tumors, Table VI). Perhaps these direct feeding arteries from carotid arteries were ringleaders for much blood loss in surgery. As we head and neck surgeons experienced few cases of extra-branches from carotid artery during neck surgery, especially neck dissection, these frequent direct branches from carotid arteries could reflect embryonic origin of branches of hereditary paraganglioma patients. As there have been few studies to report the distribution of feeding arteries into CBT, this study give the light for head and neck surgeons and interventional radiologists to deal with feeding arteries of CBT.

As our expectations, time of the surgery and the amount of blood loss depended on Shamblin classification. Shamblin III tumors took more time and blood loss than Shamblin II and I tumors during their resection surgery, while Shamblin II tumors took more time and blood loss than Shamblin I tumors (Table IV). Although effect of preoperative embolization to reduce the amount of blood loss was seen in Shamblin I and II tumors, effectiveness for reduction of time of the surgery was not obvious in our series of patients (Table V), As same results were reported by Power et al (22), it would be common that the reduction of operative time is difficult by preoperative embolization in CBT surgery. It could also be likely that the variety of embolization technique and interventional radiologists made the evaluation difficult. Multi-institutional study using standard technique must be needed to clarify the effect of preoperative embolization for accurate evaluation of the procedures.

As Shamblin III tumor surrounded ECA and ICA, resection surgery for these tumors needed resection these arteries to some extent. Actually all patients with Shamblin III tumor underwent resection of ECA and 83% of these patients (10 out of 12) underwent reconstruction of ICA in our series. Although same results were reported by some authors (23), there were few reports which mentioned about the correlation of ICA reconstruction and Shamblin III tumor. Our results indicated that preparation of reconstruction surgery of ICA must be needed to perform resection of Shamblin III CBTs.

As we performed a survey of the status of patients throughout Japan, we can report the characteristic features of CBT patients in Japan as found in our studies. There were some high-incidence areas of CBT such as Miyagi, Iwate, and Nagasaki, perhaps reflecting the prevalence of patients with a familial history of paraganglioma with some gene alterations. Among the 94 patients who underwent surgery to remove a CBT, 23 patients presented with tumors classified as Shamblin type I, 59 with type II, and 12 with type III. The most frequent feeding artery of these CBTs was the ascending pharyngeal artery. Preoperative embolization of these feeding arteries was effective to reduce blood loss, but not the operation time of Shamblin type I and II tumors.

Acknowledgements

This work was supported by a Grant-in-aid for JSPS KAKENHI (grant no. 26462619). The abstract of the present study was published in J Clin Oncol 35 (Suppl 15): e17574, 2017.

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