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Research Article: Clinical Case Report

Ectopic thyroid of the pancreas

A case report and literature review

Ma, Aiwen MD; Liu, Hongfeng MD*

Editor(s): Feigerlova., Eva

Author Information
doi: 10.1097/MD.0000000000008707
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Abstract

1 Introduction

Ectopic thyroid is a rare developmental abnormality that occurs during the migration of the thyroid anlage. It can be found anywhere along the path of the thyroid descent, from the floor of the primitive foregut to the final position of the thyroid in the neck. The estimated frequency of ectopic thyroid is 0.17 per 1000 patients,[1] with lingual thyroid accounting for 90% of cases.[2] Sublingual types are less frequently encountered, and ectopic thyroid below the diaphragm is an even more rare condition.

Experience with intraabdominal ectopic thyroid in the clinical literature is limited, and doctors could mistake ectopic thyroid tissue for neoplasms of adjacent tissues. The most appropriate management of this entity has not been established; however, surgical removal is common to exclude malignancy. We herein report a case of intraabdominal thyroid tissue located in the pancreas and review of all the reported cases of ectopic thyroid in the abdomen to provide evidence for diagnosis and treatment.

2 Case presentation

A 73-year-old woman was admitted to Peking Union Medical College Hospital in Beijing, China, with a 6-year history of recurrent mild right upper quadrant pain, which was aggravated during the past month and could no longer be relieved by painkillers (not known). She had not previously been diagnosed with any other diseases.

A retroperitoneal hyperechoic mass was detected using abdominal ultrasonography (USG). A further abdominal computed tomography (CT) scan was performed, which indicated an inhomogeneous, ovoid mass measured 60 × 50 mm; the mass was hypodense (56 HU) in comparison with the normal liver parenchyma (Fig. 1A) It had a well-defined margin with small sheet-like calcifications and cystic degeneration. The mass was surrounded by the duodenum, was in front of the inferior vena cava, and compressed the head of the pancreas. After contrast medium administration, there was obvious enhancement in the arterial phase, which was hyperdense to the liver and lasted throughout the portal and delay phases (Fig. 1B–D). The coronal axes showed the accurate location of the mass, and 3D reconstruction suggested a rich blood supply from the celiac trunk (Fig. 1E, F).

F1-48
Figure 1:
Abdominal computed tomography (CT) scan findings (black arrow). (A) Unenhanced CT showed inhomogeneous, ovoid mass (60 mm × 50 mm), with a well-defined margin and small sheetlike calcification and cystic degeneration. (B–D) The lesion demonstrates heterogeneous contrast enhancement on arterial phase (after 35–40 seconds), portal phase (after 40–60 seconds), and delay phase. (E) Coronal axes showed the location of the mass. (F) 3D reconstruction of vessels showed rich blood supply from the celiac trunk.

Fine needle aspiration cytology (FNAC) was suggested to the patient as it is a routine preoperative work-up for pancreatic neoplasms, and may have been especially useful in this difficult case. However, as the mass was deep in the retroperitoneal space and had a rich blood supply, there was a risk of hemorrhage. After a discussion, the patient refused the examination. Surgery was then performed, which revealed a mass of about 8 cm in diameter with a complete capsule. It was found between the liver and the superior border of the kidney, and had a close interaction with the pancreatic hook. The mass was totally resected with some pancreatic tissue. Postoperatively, the patient had an uneventful course.

Histological examination revealed that the lesion consisted of differentiated thyroid tissue surrounded by some pancreatic tissue, with dilation of pancreatic duct (Fig. 2A). After immunohistochemistry (IHC) staining, strong expression of thyroid transcription factor-1 (TTF-1) and thyroglobulin (TGB) was seen, while BRAFV600E was negative (Fig. 2B–D). On the basis of the morphology and IHC results, ectopic thyroid was diagnosed. Careful evaluation of the thyroid and neck lymph nodes with ultrasound revealed mixed cystic and solid thyroid nodules; as a result, there was a very low chance of malignancy. Thyroid-specific laboratory tests were normal. USG examination of the uterus and bilateral ovaries revealed no lesions. The patient refused to undergo further nuclear scintigraphy to detect ectopic thyroid tissue in other parts of the body. After 2 years of follow-up, she had no signs of relapse according to USG findings, and her thyroid hormone levels were normal. The patient consented to the publication of this case report (Table 1).

F2-48
Figure 2:
Pathology examination of specimen. (A) Hematoxylin-eosin staining revealed differentiated thyroid tissue (×100). (B–D) Immunoreactivity for TGB and TTF-1, while negativity for and BRAFV66E indicate a benign tissue (×200). TGB = thyroglobulin, TTF-1 = thyroid transcription factor-1.
T1-48
Table 1:
Ectopic thyroids in the abdomen.

3 Discussion

The most common reason for ectopic thyroid tissue is an arrest of migration or excessive descent of the thyroid anlage[3]; thus, it is most often found along the path of thyroid descent (Wölfler area).[4] Ectopic thyroid tissue in the abdomen is rare and is difficult to explain by abnormal migration as it is distant from the path of embryological development. The most common interpretation is the heterotopic differentiation of precursor cells from the foregut endoderm,[5–8] as most intraabdominal organs originate in the endodermal germ layer, which is also the case for the thyroid. An exception is ectopic thyroid tissue in the adrenal gland because the adrenal cortex originates from the mesodermal layer while the medulla originates from the ectodermal layer.[9] Developmental errors, such as congenital defects in the diaphragm leading to diaphragmatic hernias are also a possible explanation.[9] In addition, ectopic thyroid tissue could also be explained as a teratoma, which originates from a single germ cell after the first meiotic division, whose histology can show other tissue components, such as skin appendages, cartilage, and bone.[10] Moreover, pancreas and thyroid gland may demonstrate more interrelationships, as the possible contribution of insulin resistance to thyroid pathology[11] and autoimmune disease could involve both thyroid and pancreas.[12]

Another important issue is to rule out metastases from thyroid carcinoma. Distant metastases of differentiated thyroid carcinomas have been found at sites including the pancreas,[13] porta hepatitis,[14] liver,[15] and others.[16] Therefore, an extensive examination of the neck thyroid gland and neck lymph nodes should be performed. However, ectopic thyroid tissue has also been reported in patients without histologic evidence of thyroid carcinoma, which is an occult papillary carcinoma. Moreover, malignant transformation of ectopic thyroid tissue could also occur; the estimated incidence of carcinoma arising in a lingual thyroid is less than 1%.[17] To distinguish benign tissue from malignant tissue, Meyer and Steinberg[18] proposed morphologic criteria, including microscopic size, round or oval follicles, nonpapillary type, uncrowded nuclei, not enlarged, no stromal proliferation, and no psammoma bodies. In addition, IHC and molecular analysis could provide more information than morphology alone. Mutations in genes regulated by transcription factors, including TTF-1 (Nkx2-1), FOXE1, and PAX-8 could lead to thyroid dysgenesis.[19] Markers such as BRAFV600E, NRAS/KRAS, galectin-3, and HBME-1 are found in differentiated thyroid carcinoma, but not in benign nonadenomatous follicular epithelium.[9] In our patient, the morphology met the aforementioned criteria. IHC positivity for TTF-1 and TGB indicated its thyroid nature, and negativity for BRAFV600E also supported a benign finding. Compared with polymerase chain reaction, IHC analysis of BRAFV600E has an 89% sensitivity and 100% specificity.[20]

Experience with intraabdominal ectopic thyroid tissue in the clinical literature is limited. We reviewed the English literature from 1960 to 2017; a total of 34 cases were reported, including in the adrenal gland (13 cases),[9,21–30] gallbladder (8 cases),[3–6,8,31–33] porta hepatis (4 cases),[34–37] mesentery (2 cases),[38,39] pancreas (2 cases),[40,41] liver (1 case),[42] spleen (1 case),[43] retroperitoneum (1 case),[10] duodenum (1 case),[44] and jejunum (1 case).[7] Ectopic thyroid tissues in the ovary (struma ovarii) are more commonly seen, comprising 1% of all ovarian tumors and 2% to 5% of ovarian teratomas.[45] Thus, our review mainly focuses on those extremely rare entities. Our case is the 3rd found in the pancreatic region.

Of the 34 cases reported, there was a predominance of women (82.4%), which is similar to ectopic thyroid tissue found in other locations. The age at diagnosis varied from 30 weeks of gestation to 76 years of age. According to the reports, ectopic thyroid was mostly asymptomatic; however, nonspecific symptoms, such as weakness, pain, dyspnea, diarrhea, hemorrhage, and other complications, may occur depending on the different anatomic sites. Ectopic thyroid tissue of the gallbladder was usually discovered after cholecystectomy for cholecystitis, while in one case[3] it was identified preoperatively as a gallbladder neoplasm that caused recurrent right upper quadrant pain without gallstones. Another interesting case[40] illustrated an ectopic thyroid of 50 × 40 × 30 mm that was pushing up the omentum minus; we presume this might be an explanation of the dyspepsia and duodenal ulcer in the patient. Thyroid hormone levels were normal in the majority of patients, except for 2 cases. In one case,[39] a patient with a nodular colloidal goiter and hyperthyroidism no longer required antithyroid drugs after resection of the abdominal mass, indicating functional ectopic thyroid tissue. In contrast, another patient with a history of hypothyroidism did not experience any changes after resection of the ectopic thyroid.[4]

Imaging methods have been used in the diagnosis of ectopic thyroid, including high-resolution ultrasound, CT, and magnetic resonance imaging, as well as nuclear scintigraphy. Ultrasounds are excellent as the 1st approach with the color-power-Doppler technique to show hypervascularity. Further unenhanced CT scans could show a characteristic uniform high attenuation[46] of the ectopic tissue because of the intrinsic iodine content. Reported Hounsfield units were 56 HU in our study, 43 HU in a study by Liang et al,[3] 59 HU in a study by Tada et al,[22] and 20 HU as reported by Takao et al.[26] Normal thyroid gland measured around 100 HU in our hospital, higher than these ectopic tissues. Notably, most adrenal gland ectopic thyroid tissues were described as cystic lesions,[22] whereas those around the porta hepatis were usually solid or semisolid masses with cystic components.[3,34,39,47] Since HU value was average, they were not exactly comparable to normal thyroid gland. All the reported ectopic thyroid tissues exhibited well-defined borders, and some had small calcifications.[21,24,28,34] After contrast medium administration, the tissues mostly showed inhomogeneous enhancement,[10,21,34,35,41,42] except for in the study by Liang et al, where they showed no obvious enhancement.[3] Presentations on magnetic resonance imaging were not uniform, showing low to high signal intensity on either T1WI or T2WI,[9,10,22,30] depending on the gelatinous colloid material; low signal intensity on T2WI was likely to correspond with highly gelatinous material.[22] Combining the aforementioned imaging methods with positron emission tomography-CT scan could help to rule out malignancy.

FNAC and core biopsy are suggested for use in preoperative diagnosis, especially for pancreatic neoplasms. Only 3 cases have involved FNAC preoperatively, 2 of which showed typical thyreocytes and follicles,[34,42] while the other found small, round epithelial cells with slightly hyperchromatic nuclei that indicated malignancy[39]; however, the final pathology was benign.

Scintigraphy using 123I, 131I, or 99mTc-pertechnetate has tissue specificity that could be used to confirm the thyroid nature of the mass, as well as to show eutopic thyroid. However, it may have limitations with regard to nonfunctional ectopic thyroid tissue.[48] In addition, give the rarity of intraabdominal ectopic thyroid tissue, scintigraphy was usually performed after biopsy or postoperatively to evaluate the presence of eutopic thyroid and demonstrate ectopic thyroid tissue in additional locations. Of the 34 cases, only 6 cases involved whole-body nuclear scintigraphy; in one case,[34] scintigraphy was performed after FNAC, while in the other cases it was performed postoperatively.[21,27,32,35,43]

For the symptomatic ectopic thyroid, the choice of treatment depends on the symptoms, size and location of the mass, histological findings, and thyroid function.[2] Surgical intervention should be applied in cases with severe obstruction, bleeding, ulceration, or suspicion of malignancy. If ectopic thyroid tissue is diagnosed, it is important to confirm the presence of a normally located thyroid gland before removing the ectopic tissue. In one case reported by Ghanem et al,[34] dual ectopia was discovered at the porta hepatis and lingua, without a gland at the thyroid bed. Only the intraabdominal ectopic thyroid was resected, and the patient received thyroid hormone replacement postoperatively to maintain euthyroidism with suppressed thyroid-stimulating hormone level. The prognosis mainly depends on the coexisting lesion. Patients who underwent simple resection of intraabdominal ectopic thyroid tissue had an uneventful postoperative recovery, without relapse or metastasis.

4 Conclusion

In our case, although ectopic thyroid tissue is benignus, it had a tendency to get enlargement and cause compression symptoms. Imaging procedures revealed a retroperitoneal mass with a well-defined border; this showed high attenuation on an unenhanced CT scan and obvious enhancement throughout the 3 phases. In postoperative pathological examination, the thyroid nature could be demonstrated by morphology as well as immunoreactivity for TGB and thyroid-restricted transcription factors (TTF-1, PAX8, and FOXE1). Negativity for BRAFV66E, NRAS/KRAS, galectin-3, and HBME-1 would also indicate a benign tissue. Polymerase chain reaction could increase the sensitivity of detection. Further detection of other ectopic thyroid tissue using USG and nuclear scintigraphy is suggested in such cases.

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Keywords:

ectopic thyroid; pancreas; thyroid gland

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