1.Diagnosis and substaging of pT1 bladder cancer.
Liang CHENG ; Wen-bin HUANG ; Su-qin ZHENG ; Jie ZHENG
Chinese Journal of Pathology 2007;36(9):636-639
2.A Case of Combined Hepatocellular-Cholangiocarcinoma with Underlying Schistosomiasis.
Chang Kyun HONG ; Jin Mo YANG ; Bong Koo KANG ; Jin Dong KIM ; Young Chul KIM ; U Im CHANG ; Jin Young YOO
The Korean Journal of Internal Medicine 2007;22(4):283-286
Combined hepatocellular-cholangiocarcinoma is a rare form of primary liver cancer showing features of both hepatocellular and biliary epithelial differentiation. We report here on a case with collision tumor, which apparently was the coincidental occurrence of both hepatocellular carcinoma and cholangiocarcinoma underlying schistosomiasis. A 39-year-old-Philippine female was transferred to our hospital for evaluation of a liver mass that was found on ultrasonography at a local hospital. HBsAg and Anti-HCV were negative and serum alpha-fetoprotein (AFP) level was normal. The tumor mass was histologically diagnosed as adenocarcinoma by sono-guided biopsy before the operation. Partial lobectomy was performed and we histologically identified the concurrent occurrence of hepatocellular carcinoma and cholangiocarcinoma, (a "collision type carcinoma").
Adenocarcinoma/diagnosis/pathology/surgery
;
Adult
;
Carcinoma, Hepatocellular/*diagnosis/pathology/surgery
;
Cholangiocarcinoma/*diagnosis/pathology/surgery
;
Female
;
Humans
;
Schistosomiasis/*physiopathology
3.Papillary thyroid microcarcinoma.
Peng XIE ; Honfu DENG ; Tianzhi TAN
Journal of Biomedical Engineering 2009;26(5):1167-1170
The recent prevalence of ultrasonography (US) and US-guided fine needle aspiration biopsy (FNAB) can make us easily diagnose papillary carcinoma of 1.0 cm or less in maximal diameter, which is called papillary microcarcinoma. In the face of the fact that cervical lymph node metastasis and multicentricity are two prominent clinical characteristics of papillary thyroid microcarcinoma, the question How to treat papillary microcarcinoma has given rise to controversy. In this review, we discuss the clinical behavior, the appropriate therapeutic strategies, the factors affecting prognosis, and the methods for following up the patients with papillary thyroid microcarcinoma.
Biopsy, Fine-Needle
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Carcinoma, Papillary
;
diagnosis
;
pathology
;
surgery
;
Humans
;
Prognosis
;
Thyroid Neoplasms
;
diagnosis
;
pathology
;
surgery
5.Emphasis on diagnosis of thyroid carcinoma.
Chinese Journal of Pathology 2014;43(5):289-290
6.Cytology diagnosis and clinical management of fine-needle aspiration for thyroid nodules.
Jin-yu ZHENG ; Tao BAI ; Yi-fen ZHANG ; A-qing CHEN ; Qin HUANG
Chinese Journal of Pathology 2010;39(5):349-352
Biopsy, Fine-Needle
;
Carcinoma
;
diagnosis
;
pathology
;
surgery
;
Carcinoma, Medullary
;
diagnosis
;
pathology
;
surgery
;
Carcinoma, Papillary
;
diagnosis
;
pathology
;
surgery
;
Carcinoma, Papillary, Follicular
;
diagnosis
;
pathology
;
surgery
;
Diagnosis, Differential
;
Goiter, Nodular
;
diagnosis
;
pathology
;
therapy
;
Hashimoto Disease
;
diagnosis
;
pathology
;
therapy
;
Humans
;
Lymphoma
;
diagnosis
;
pathology
;
surgery
;
Thyroid Nodule
;
pathology
;
surgery
;
Thyroidectomy
7.Diagnosis of Pancreatic Intraductal Papillary Mucinous Neoplasm.
The Korean Journal of Gastroenterology 2008;52(4):207-213
Intraductal papillary mucinous neoplasm (IPMN) of the pancreas is a unique disease entity that is characterized by predominant intraductal growth of mucinous cells, copious mucin production, and subsequent cystic dilatation of pancreatic ducts. IPMN shows a spectrum of histologic and imaging findings and possesses as the potential for malignant transformation arising from adenoma to invasive carcinoma. It is important to determine the type, extent of duct involvement, and presence of malignant transformation, and to assess tumor grading prior to surgical resection. Thus, it would be helpful for physicians managing patients with IPMN of the pancreas to have a guideline for the diagnosis and treatment of IPMN. In this review, a role of radiological evaluation for diagnosis and preoperative assessment is described as well as presentation of the guideline for patient management.
Adenocarcinoma, Mucinous/*diagnosis/pathology/surgery
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Carcinoma, Pancreatic Ductal/*diagnosis/pathology/surgery
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Carcinoma, Papillary/*diagnosis/pathology/surgery
;
Diagnosis, Differential
;
Humans
;
Magnetic Resonance Imaging
;
Pancreatic Neoplasms/*diagnosis/pathology/surgery
;
Preoperative Care
;
Prognosis
;
Tomography, X-Ray Computed
8.An unusual appearance of renal epithelioid angiomyolipoma.
Chee-Wai MAK ; Jin Ming CHANG ; Wen Sheng TZENG ; Steve K HUAN
Singapore medical journal 2012;53(10):e204-7
Epithelioid angiomyolipoma is a recently described rare variant of renal angiomyolipoma. It can occur in patients with or without tuberous sclerosis. We report the imaging findings of a case of epithelioid angiomyolipoma that showed the presence of fatty tissue undifferentiated from the typical angiomyolipoma at the beginning. After partial nephrectomy, tumour recurrence occurred two years later, presenting as completely solid tumours with no adipose tissue, and with invasion into the psoas muscle and left adrenal gland. Differentiation of this tumour from renal cell carcinoma is difficult. Both the radiologist and surgeon should be aware of the existence of this tumour and its potentially malignant behaviour.
Aged
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Angiomyolipoma
;
diagnosis
;
pathology
;
surgery
;
Carcinoma, Renal Cell
;
diagnosis
;
Diagnosis, Differential
;
Female
;
Humans
;
Kidney
;
pathology
;
Kidney Neoplasms
;
diagnosis
;
pathology
;
surgery
;
Neoplasm Recurrence, Local
;
pathology
;
Tomography, X-Ray Computed
9.Diagnosis and treatment of rare malignant tumors in external auditory canal.
Fangyuan WANG ; Nan WU ; Zhaohui HOU ; Jun LIU ; Weidong SHEN ; Weiju HAN ; Shiming YANG
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2015;29(16):1438-1442
OBJECTIVE:
To analyze the diagnosis, therapy and prognosis of the rare cases of malignant tumors in external auditory canal.
METHOD:
Eight cases of rare malignant tumors in external auditory canal were collected except squamous cell carcinoma and adenoid cystic carcinoma. The clinical manifestation, staging, surgical method, secondary treatment and prognosis were analysed.
RESULT:
There were 5 cases of basal cell carcinoma and 2 cases of mucoepidermoid carcinoma and 1 case of myoepithelial carcinoma. Three cases of the 5 basal cell carcinoma in external auditory canal have been misdiagnosed for a long time. After admission, 4 of the 5 basal cell carcinoma were T1 stage and cured only by a complete resection of tumor. One case of T2 stage basal cell carcinoma was found recurrence 2 years later after the first excision of tumor, and was treated with radiotherapy. Tumor was controlled. Two cases of mucoepidermoid carcinoma had been misdiagnosed as a benign tumor and received a resection. One case was found metastasis to the parapharyngeal space and nasopharynx and was treated with concurrent chemotherapy. Tumor was also controlled after 5-years follow-up. Another case was found metastasis to parotid gland and received an expanding tumor resection. No recurrence was detected after a 1-year followed up. One case of T4 stage myoepithelial carcinoma in external auditory canal was a metastasis of parotid and received a partial temporal bone resection. No-recurrence was found 1 year later.
CONCLUSION
Because the tumors above have a very low incidence in external ear canal and the location of tumors are hidden, they are often misdiagnosed and delayed in treatment. Therefore, otologists should pay more attention to avoid the misdiagnosis. To the treatment, complete surgical resection of early-stage tumor is important and for late-stage tumor, a supplemented by chemoradiotherapy may be needed.
Carcinoma, Adenoid Cystic
;
diagnosis
;
surgery
;
Carcinoma, Basal Cell
;
diagnosis
;
surgery
;
Carcinoma, Squamous Cell
;
diagnosis
;
surgery
;
Ear Canal
;
pathology
;
Ear Neoplasms
;
diagnosis
;
surgery
;
Humans
;
Neoplasm Recurrence, Local
;
Neoplasm Staging
;
Parotid Gland
;
pathology
;
Prognosis
;
Retrospective Studies
;
Temporal Bone
;
surgery
10.Surgical Management of Intraductal Papillary Mucinous Neoplasms.
The Korean Journal of Gastroenterology 2008;52(4):220-225
With increasing indence and peculiar clinico-pathological features, intraductal papillary mucinous neoplasm (IPMN) of the pancreas has been a major interest in the field of pancreatology. Although pathologic and clinical diversities make difficulty in decision of treatment of IPMN in some circumstances, surgical treatment is generally indicated for main duct IPMN and branch duct IPMN with suspected malignancy (tumor size >or=30 mm, mural nodules, dilated main pancreatic duct, or positive cytology) or prominent symptoms. IPMN has a favorable prognosis after the resection. However, invasive IPMN shows poor prognosis comparable to stage-matched pancreatic ductal adenocarcinoma. Conventional pancreatic resection is recommended in case of highly suspected malignant cases, and organ preserving pancreatectomy or minimal invasive surgery could be used, especially in benign looking branch duct IPMN. Before the surgical resection, clinician should consider patient's general and social condition as well as risk of malignancy to select proper type and extent of surgery.
Adenocarcinoma, Mucinous/diagnosis/pathology/*surgery
;
Carcinoma, Pancreatic Ductal/diagnosis/pathology/*surgery
;
Carcinoma, Papillary/diagnosis/pathology/*surgery
;
Humans
;
*Pancreatectomy
;
Pancreatic Neoplasms/diagnosis/pathology/*surgery
;
Preoperative Care
;
Survival Analysis
;
Treatment Outcome