scholarly journals Gross Hematuria and Bladder Tumor in a Patient with Advanced Thyroid Papillary Carcinoma

2013 ◽  
Vol 2013 ◽  
pp. 1-3
Author(s):  
Takao Ando ◽  
Yuki Matsuo ◽  
Toshiyuki Ikeoka ◽  
Kojiro Oba ◽  
Yasuyoshi Miyata ◽  
...  
Keyword(s):  
Thyroid Carcinoma ◽  
Papillary Carcinoma ◽  
Bladder Tumor ◽  
Clinical History ◽  
Thyroid Papillary Carcinoma ◽  
Pathological Examination ◽  
Gross Hematuria ◽  
Thyroid Papillary ◽  
History Of ◽  
Carcinoma Metastasis

We present a 73-year-old female with advanced thyroid papillary carcinoma who complained of gross hematuria. We found a bladder tumor and considered it the cause of her symptom. Cystoscopic findings of the tumor were unusual, with peri-tumor vessel formation. Pathological examination of the bladder tumor was consistent with metastasis of thyroid papillary carcinoma. Therefore, we identified thyroid carcinoma metastasis to the urinary bladder as the cause of hematuria in our patient. Thyroid carcinoma metastasis to the bladder is extremely rare, but it should be included among differential diagnoses for gross hematuria in patients with a clinical history of thyroid carcinoma.

Thyroid Papillary Carcinoma in a 3-year-old American Boy with a Family History of Thyroid Cancer

2010 ◽  
Vol 32 (3) ◽  
pp. e118-e121 ◽  
Author(s):  
Lovedeep Khara ◽  
Adam Silverman ◽  
Colin Bethel ◽  
Cyril DʼCruz ◽  
Xinlai Sun
Keyword(s):  
Thyroid Cancer ◽  
Family History ◽  
Papillary Carcinoma ◽  
Thyroid Papillary Carcinoma ◽  
Thyroid Papillary ◽  
History Of

Primary Localized Cutaneous Amyloidosis in Association with Papillary Thyroid Carcinoma

2002 ◽  
Vol 6 (4) ◽  
pp. 332-334 ◽  
Author(s):  
Yoshiko Sangen ◽  
Akira Kawada ◽  
Akira Maeda ◽  
Yoshinori Aragane ◽  
Tadashi Tezuka
Keyword(s):  
Papillary Thyroid Carcinoma ◽  
Skin Lesion ◽  
Thyroid Carcinoma ◽  
Papillary Carcinoma ◽  
Thyroid Papillary Carcinoma ◽  
Cutaneous Manifestation ◽  
Papillary Thyroid ◽  
Salmon Pink ◽  
Thyroid Papillary ◽  
Clinical Pictures

Background: Lichen amyloidosis, a type of primary localized cutaneous amyloidosis, is characterized by pruritic brown or grayish pigmented papules. Objective: We report a case of lichen amyloidosis in which the skin lesion consisted of asymptomatic salmon-pink-colored papules on the back of the neck to the upper back. This was different from typical clinical pictures of lichen amyloidosis. Our patient proved to have thyroid papillary carcinoma. Conclusion: Our case may suggest that lichen amyloidosis could be a cutaneous manifestation of thyroid cancers.

scholarly journals The first case of papillary thyroid carcinoma in an adolescent with congenital dyshormonogenetic hypothyroidism in Serbia

2014 ◽  
Vol 71 (11) ◽  
pp. 1078-1080 ◽  
Author(s):  
Jelena Eremija ◽  
Tatjana Milenkovic ◽  
Katarina Mitrovic ◽  
Sladjana Todorovic ◽  
Rade Vukovic ◽  
...  
Keyword(s):  
Thyroid Carcinoma ◽  
Papillary Carcinoma ◽  
Differentiated Thyroid Carcinoma ◽  
Pathological Examination ◽  
Pediatric Malignancy ◽  
First Case ◽  
Thyroid Papillary ◽  
Right Lobe ◽  
The Right

Introduction. Differentiated thyroid carcinoma (DTC) is a rare childhood malignancy, as it represents 0.3-0.4% of pediatric malignancies. Papillary carcinoma is the most common type of pediatric DTC and it represents about 90% of all DTC patients. Although rare, DTC arising from dyshormonogenetic goiter is the most serious complication of congenital hypothyroidism. Case report. We presented the development of thyroid papillary carcinoma in a 15-year-old girl diagnosed with congenital dyshormonogenetic hypothyroidism at neonatal age. Considering the early initiation and proper dosage of hormonal substitution, normal levels of thyreotropin and thyroid hormones were achieved quickly and maintained through a follow-up period. The girl remained euthyroid and asymptomatic until 13.8 years of age, when she presented with a large multinodular goiter. The patient underwent total thyroidectomy. Pathological examination revealed intrathyroid microcarcinoma in the right lobe. Conclusion. Although differentiated thyroid carcinoma is a rare pediatric malignancy, it is of great importance to have a certain degree of clinical caution and provide a multidisciplinary approach during the follow-up of patients with dyshormonogenetic hypothyroidism.

scholarly journals Pneumatosis intestinalis in a radioactive iodine-refractory metastasic thyroid papillary carcinoma with BRAFV600E mutation treated with dabrafenib–trametinib: a case report

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
M. C. Martín-Soberón ◽  
S. Ruiz ◽  
G. De Velasco ◽  
R. Yarza ◽  
A. Carretero ◽  
...  
Keyword(s):  
Case Report ◽  
Papillary Carcinoma ◽  
Radioactive Iodine ◽  
Specific Treatment ◽  
Pneumatosis Intestinalis ◽  
Thyroid Papillary Carcinoma ◽  
Intestinal Pneumatosis ◽  
Abdominal Symptoms ◽  
Positron Emission ◽  
Thyroid Papillary

Abstract Background Pneumatosis intestinalis (PI) is a rare entity which refers to the presence of gas within the wall of the small bowel or colon which is a radiographic sign. The etiology and clinical presentation are variable. Patients with PI may present either with chronic mild non-specific symptoms or with acute abdominal pain with peritonitis. Some cases of intestinal pneumatosis have been reported as adverse events of new oncological treatments such as targeted therapies that are widely used in multiple tumors. Case presentation A 59-year-old caucasian female with radioactive iodine-refractory metastatic thyroid papillary carcinoma with BRAFV600E mutation was treated with dabrafenib and trametinib as a compassionate use. After 4 months treatment, positron emission tomography–computed tomography (PET–CT) showed PI. At the time of diagnosis, the patient was asymptomatic without signs of peritonitis. The initial treatment was conservative and no specific treatment for PI was needed. Unfortunately, after dabrafenib–trametinib withdrawal, the patient developed tumor progression with significant clinical worsening. Conclusions This case report is, in our knowledge, the first description of PI in a patient treated with dabrafenib–trametinib. Conservative treatment is feasible if there are no abdominal symptoms.

scholarly journals ResCaps: an improved capsule network and its application in ultrasonic image classification of thyroid papillary carcinoma

2021 ◽  
Author(s):  
Xiongzhi Ai ◽  
Jiawei Zhuang ◽  
Yonghua Wang ◽  
Pin Wan ◽  
Yu Fu
Keyword(s):  
Papillary Carcinoma ◽  
Network Model ◽  
Reliability And Validity ◽  
Thyroid Papillary Carcinoma ◽  
Data Set ◽  
Ultrasonic Image ◽  
First Choice ◽  
Thyroid Papillary ◽  
Ultrasonic Images

AbstractUltrasonic image examination is the first choice for the diagnosis of thyroid papillary carcinoma. However, there are some problems in the ultrasonic image of thyroid papillary carcinoma, such as poor definition, tissue overlap and low resolution, which make the ultrasonic image difficult to be diagnosed. Capsule network (CapsNet) can effectively address tissue overlap and other problems. This paper investigates a new network model based on capsule network, which is named as ResCaps network. ResCaps network uses residual modules and enhances the abstract expression of the model. The experimental results reveal that the characteristic classification accuracy of ResCaps3 network model for self-made data set of thyroid papillary carcinoma was $$81.06\%$$ 81.06 % . Furthermore, Fashion-MNIST data set is also tested to show the reliability and validity of ResCaps network model. Notably, the ResCaps network model not only improves the accuracy of CapsNet significantly, but also provides an effective method for the classification of lesion characteristics of thyroid papillary carcinoma ultrasonic images.

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