• 대한핵의학회지
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• 제25권2호
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• pp.280-285
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• 1991

We analyzed Radioisotope scan findings of 46 patients of thyroiditis which were proven pathologically at K.C.H. The results were as follows 1) 45 patients were female, one was male and average age of patients was 37 years old. 2) The lesion site was predominant in both lobe (67%) 3) Hashimoto's thyroiditis showed enlarged thyroid (85%) with cold nodule (20%), diffuse decreased activity (10%), while subacute thyroiditis was presented absent activity (53%), poor visualization (20%) or cold nodule (7%) 4) Radioisotope scan was valuable in evaluations function of thyroid gland and detection of lesion but there was a limit of pathological nature.

• 대한핵의학회지
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• 제30권1호
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• pp.65-76
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• 1996

1993년 2월부터 1994년 8월까지 경북대학교병원 핵의학과에서 진료한 갑상선질환 중 그레이브스병 402예와 하시모토갑상선염 230예를 대상으로 혈청 thyrotropin-binding inhibiting immunoglobulin (TBII)치를 방사면역측정법으로 측정하여 갑상선 기능상태와 그 치료경과에 있어서의 동태를 관찰하고 아울러 혈청 갑상선글로블린치, antithyroglobulin anti-body(ATAb) 및 antimicrosomal antibody(AMAb)의 동태를 동시에 검토하여 다음과 같은 결과를 얻었다. 혈청 TBII치는 갑상선기능항진성 그레이브스병에서 평균 $40.82{\pm}21.651%$, 하시모토갑상선염에서 평균 $8.89{\pm}14.522%$로서 정상 대조군의 평균 $3.21{\pm}2.571%$에 비하여 유의한 상승치를 보였다. 그레이브스병 중에서도 갑상선기능항진증이 있는 387예에서는 TBII치가 비정상적으로 증가한 예가 92.2%(357예)였으며, 갑상선기능이 정상으로 회복된 그레이브스병 15예에서는 TBII치가 비정상적으로 증가된 예는 46.7%(7예)에 불과하였다. 하시모토갑상선염 230예에서는 TBII치가 비정상적으로 상승한 예는 23.9%(55예)였다. 그레이브스병에서 TBII치들은 RAIU 6시간치 및 24시간치, T3, T4, FT4들과 유의한 양의 상관성을 나타내었으며, 혈청 갑상선글로블린 및 AMAb와도 양의 상관성을 나타내었다(p<0.001). 그러나 혈청 TBII치와 TSH와는 음의 상관성을 나타내었고(p<0.001), ATAb와는 상관성이 없었다. 하시모토갑상선염에서는 TBII치는 RAIU 6시간치 및 24시간치, T3, TSH, AMAb와는 유의한 양의 상관성이 있었고(p<0.05), 혈청 T4, FT4, 갑상선글로불린 및 ATAb치와는 상관성이 없었다. 결론적으로, 그레이브스병에서는 혈청 TBII치가 갑상선기능항진증의 정도를 반영하는 소견이 되며 회복기의 TBII치는 예후를 반영하는 자료가 될 수 있다. 그리고 하시모토갑상선염에서는 비록 TBII치가 상승된 예는 많지 알지만 갑상선기능이 항진되거나 저하되는 소견의 정도와 관련이 있고 병변의 중증도를 반영한다고 볼 수가 있다.

• 대한의생명과학회지
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• 제10권3호
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• pp.211-217
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• 2004

For discrimination of ductal and ascinar cells, we isolated a single-chain variable domain fragment (scFv) antibody against ductal cells of salivary gland using phage display technique. From the spleen of a mouse immunized with ductal cell lysate, total RNA was prepared and used as a template for cDNA synthesis of antibody genes. The scFv genes were constructed with variable domain genes of heavy and light chain and were introduced into pCANTAB5E to construct phage scFv library. The phage particles specific for acinar cells were screened by subtraction using immunotubes coated with acinar and ductal cell lysate and enzyme-linked immunoabsorbance assay (ELISA). The characteristics of the scFv were determined by immunohistochemistry (IHC) and the result indicated that the isolated scFv has the specificity against ductal cells of salivary glands and tubules of kidney. And the scFv has an unique binding activity specific for Hashimoto's thyroiditis. The nucleotide sequence of isolated scFv gene was determined and revealed that V/sub H/ belongs to the mouse H-chain family subgroup IB and V/sub L/ to the mouse L-chain family subgroup III.

• 대한한방내과학회지
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• 제39권4호
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• pp.645-661
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• 2018

Objectives: The aim of this paper was to aid Korean clinical practices for determining clinical and subclinical hypothyroidism and to identify further relevant studies by summarizing the present domestic clinical studies. Methods: The research consisted of a review of articles up to July, 2018 found by searching 'Hypothyroidism' and 'Hashimoto's thyroiditis' as keywords in five domestic electronic databases. Results: Only nine studies satisfied the selection criteria and were analyzed. These included six case reports, two controlled clinical trials, and one randomized controlled trial. Of these, Anjeonleejoong-tang was the most frequent herbal medicine used to treat hypothyroidism. Conclusions: Systematic and large-scale research studies are needed to standardize the guidelines for traditional Korean treatment of hypothyroidism.

• Journal of Yeungnam Medical Science
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• 제31권2호
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• pp.127-130
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• 2014

Autoimmune thyroiditis is the most common cause of hypothyroidism in the world. It is characterized clinically by gradual thyroid failure, goiter formation, or both, because of the autoimmune-mediated destruction of the thyroid gland. Renal involvement presenting proteinuria in autoimmune thyroiditis is not uncommon, occurring in 10% to 30% of the cases. Glomerulonephropathy associated with autoimmune thyroiditis, however, is a rare disease. Most reports of autoimmune thyroiditis with glomerulonephropathy have demonstrated a mixed pathological morphology and have been predominantly associated with membranous glomerulopathy. The case of minimal-change disease associated with thyroiditis presenting acute kidney injury is a rare disease that has not been reported in South Korea. Reported herein is the case of a 16-year-old man diagnosed with Hashimoto's thyroiditis, with minimal-change disease presenting acute kidney injury. He revealed hypothyroidism, proteinuria, and impaired renal function. Renal biopsy showed minimal-change disease and minimal tubular atrophy. The patient was treated with thyroid hormone, and his renal function and proteinuria improved. Therefore, for patients with autoimmune thyroiditis presenting unexplained proteinuria, glomer-ulonephropathy should be ruled out. Conversely, for patients with glomerulonephropathy and persistent proteinuria despite proper treatment, thyroid function and antibody tests should be performed.

• Journal of Yeungnam Medical Science
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• 제27권2호
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• pp.165-172
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• 2010

저자들은 최근 원발성 갑상선 림프종으로 진단한 3예를 경험하였기에 이를 문헌고찰과 함께 보고하는 바이다. 특히 증례 3에서와 같이 전경부 종괴로 내원한 환자에서 과거 하시모토 갑상선염의 병력이 없더라도 갑상선초음파에서 하시모토갑상선염을 의심할 수 있는 갑상선실질의 미만성 변화를 보이고, 실질 부위와 구분되는 명확한 거대한 저에코성 종괴를 보이는 경우 갑상선 림프종을 감별 진단하여야 할 것으로 생각되며, 우선적으로 초음파 유도하 세침흡인검사를 실행하고, 확진을 위해 조직생검을 하여야 할 것으로 생각된다.

• Asian Pacific Journal of Cancer Prevention
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• 제16권6호
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• pp.2447-2451
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• 2015

Background: Human papillary thyroid carcinoma (PTC) is often associated with Hashimoto's thyroiditis (HT); their coexistence improves PTC prognosis. Osteopontin, a secreted glycoprotein, plays a role in cell survival, immunity, and tumor progression, its expression being associated with a poor prognosis and metastasis in several malignancies. Osteopontin overexpression correlates with aggressive clinicopathological features in PTC. Lymph node metastases and large tumor size positively correlate with osteopontin positivity. This study aimed to: (1) confirm osteopontin overexpression in human PTC samples; (2) compare osteopontin expression levels in PTC cases with and without HT; and (3) identify correlations between tumor aggressiveness and osteopontin expression levels. Materials and Methods: Plasma osteopontin was assessed in 45 patients with PTC, 22 patients with PTC and HT, and 24 healthy controls by enzyme-linked immunosorbent assay. Thyroid tissue osteopontin mRNA and protein levels were analyzed by reverse transcription-polymerase chain reaction and Western blotting, respectively. Results: Plasma osteopontin levels were significantly higher in PTC patients than in healthy controls. Plasma osteopontin, tissue osteopontin mRNA, and tissue osteopontin protein levels were significantly lower in patients with PTC and HT than in those with PTC alone. In advanced disease stage cases, osteopontin mRNA and protein expression levels were lower in patients with PTC and HT than in those with PTC alone. However, the osteopontin expression level was not significantly associated with the TNM stage. Conclusions: Plasma osteopontin, tissue osteopontin mRNA, and tissue osteopontin protein levels were significantly lower in patients with PTC and HT than in those with PTC alone, suggesting that HT attenuates PTC aggressiveness through negative regulation of osteopontin expression.

• 대한세포병리학회지
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• 제8권2호
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• pp.150-154
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• 1997

Lymphoid infiltration can be seen in some lesions such as Hashimoto's thyroiditis, subacute thyroiditis and several neoplasm of the thyroid. In case of malignancy, there are a few reports of lymphoid infiltration in the diffuse sclerosing variant of papillary carcinoma. But heavy lymphoid infiltraton without evidence of sclerosis is uncommon. We experienced a case of papillary oxyphilic carcinoma with massive lymphoid infiltration, which looks like Warihin tumor of salivary gland. However cytological feature of epithelial cells exhibit that of papillary carcinoma.

• Asian Pacific Journal of Cancer Prevention
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• 제16권3호
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• pp.1135-1138
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• 2015

Background: The objective of this study was to investigate the MSCT characteristics of PTL in order to enhance the awareness of this uncommon entity among both clinicians and radiologists. Materials and Methods: The clinicopathological data and MSCT images of 27 patients with PTL were retrospectively reviewed. The MSCT appearances were classified into three types: type 1, solitary nodule surrounded by normal thyroid tissue; type 2, multiple nodules in the thyroid, and type 3, enlarged thyroid glands with a reduced attenuation with or without peripheral thin hyperattenuating thyroid tissue. Results: The patients were enrolled in the study with a mean age of 68 years (range, 51-86years) and compression symptoms or enlarged cervical lymph nodes at diagnosis. Hashimoto's thyroiditis was in 20 patients. All patients had non-Hodgkin lymphoma of B-cell in origin, including 22 cases of diffuse large B-cell lymphoma (DLBCL) and 5 of low-grade B-cell lymphoma of mucosa-associated lymphoid tissue (MALT). For MSCT appearance, type 1 pattern was observed in 2 patients, type 2 in 8, and seventeen type 3 in 17. The lesions occurred in more than one lobe with a mean maximal transverse diameter of 6.9 cm and an ill-defined margin. Most tumors showed a homogeneous attenuation equal to that of surrounding muscles before contrast and obvious enhancement after contrast. Cervical lymph node involvement and invasion of the trahea and (or) esophagus were mainly observed in patients with DLBCL. Conclusions: PTL should be clinically considered in elder patients presenting with a history of Hashimoto's thyroiditis and cervical lymphadenopathy. The MSCT characteristics of PTL includes a mass diffusely affecting more than one thyroid lobe, isointense to muscle and obvious enhancement before and after contrast. DLBCL, the most common histological subtype of PTL, is associated with a higher invasive tendency.

• 대한영상의학회지
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• 제81권5호
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• pp.1250-1254
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• 2020

미만성 경화 변종 갑상선 유두암은 갑상선 유두암의 드문 변종이다. 저자들은 통증을 동반하지 않은 미만성 갑상선 비대를 보였던 9세 여자 환아에서 발생한 미만성 경화 변종 갑상선 유두암의 드문 증례에 대해 보고하고자 한다. 환아는 갑상선 과산화효소 항체에 양성이었고, 처음에는 하시모토 갑상선염으로 진단받았다. 하지만 갑상선 초음파 상에서 미만성 경화 변종 갑상선 유두암의 특징적인 초음파 소견을 보였고, 수술 후 미만성 경화 변종 갑상선 유두암으로 확진되었다. 비록 소아에서 갑상선암은 드물지만 갑상선 비대를 보일 때 미만성 경화 변종 갑상선 유두암의 가능성을 고려해야 한다. 또한 초음파를 시행함으로써 갑상선암의 진단이 지연되는 것을 막을 수 있다.