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Protein Expression of Cyclin B1, Transferrin Receptor, and Fibronectin Is Correlated with the Prognosis of Adrenal Cortical Carcinoma

Moon SJ, Kim JH, Kong SH, Shin CS

BACKGROUND: Adrenal cortical carcinoma (ACC) is a rare cancer with a variable prognosis. Several prognostic factors of ACC have been previously reported, but a proteomic analysis has not yet been...
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Estrogen-secreting adrenocortical carcinoma

Jeong Y, Cho SC, Cho HJ, Song JS, Kong JS, Park JW, Ku YH

Adrenocortical carcinoma is a rare type of endocrine malignancy with an annual incidence of approximately 1–2 cases per million. The majority of these tumors secrete cortisol, and a few secrete...
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An Intrarenal Adrenocortical Carcinoma Arising in an Adrenal Rest

Lee JH, Choi YD, Cho NH

We describe a case of a 61-year-old Korean man who was diagnosed with renal cell carcinoma that was discovered on abdominopelvic computed tomography obtained after the patient complained of back...
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Myxoid and Sarcomatoid Variants of Adrenocortical Carcinoma: Analysis of Rare Variants in Single Tertiary Care Center

Sung TY, Choi YM, Kim WG, Lee YM, Kim TY, Shong YK, Kim WB, Song DE

The aim of this study is to describe rare variants of adrenocortical carcinoma (ACC) and to compare the prognosis with that of conventional ACC. We retrospectively reviewed 8 cases of...
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Imaging of F-18 FDG PET/CT and follow up of bilateral invasive adrenal diffuse large B cell lymphoma mimicking adrenocortical carcinoma

Shim HK, Kim SW

The incidence of malignant adrenal tumors, including primary adrenal lymphoma (PAL) and adrenocortical carcinoma (ACC), is rather low. Early differentiation between ACC and PAL is necessary because the therapeutic strategies...
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Virilizing Adrenocortical Carcinoma Advancing to Central Precocious Puberty after Surgery

Kim MS, Yang EJ, Cho DH, Hwang PH, Lee DY

Adrenocortical carcinoma (ACC) in pediatric and adolescent patients is rare, and it is associated with various clinical symptoms. We introduce the case of an 8-year-old boy with ACC who presented...
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A Case of Recurrent Adrenocortical Carcinoma with Stomach Metastasis

Park JS, Kim HJ, Lee SH, Choi YW, Yim HE, Ahn MS

Adrenocortical carcinoma (ACC) is a rare disease with poor prognosis. We experienced a case of recurrent ACC with stomach metastasis which had been completely cured a long while ago. A...
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Surgical Outcomes of Adrenocortical Carcinoma; 20 Years of Experience in a Single Institution

Kim MJ, Ban EJ, Jung SJ, Son HY, Lee CR, Kang SW, Jeong JJ, Nam KH, Chung WY, Park CS

PURPOSE: Adrenocortical carcinoma (ACC) is a rare malignant tumor. Early detection is difficult and prognosis is poor. We report on 20 years of ACC surgical experience at our institution. METHODS: This...
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A Case of an Adrenocortical Carcinoma with Pulmonary Embolism as the Initial Manifestation

Lee HJ, Kwak JY, Kim YJ, Kim TH, Lee JD, Lee HW, Kim HJ, Kim DJ, Chung YS, Lee KW, Han SJ

The annual incidence of a first episode of deep vein thrombosis or pulmonary embolism (PE) in the general population is 120 per 100,000. Cancer is associated with an approximately 4-...
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A Case of Adrenocortical Carcinoma Secreting Cortisol and Aldosterone

Ha J, Kim MK, Cha YJ, Kim SK, Yun GY, Rhee K, Park JS, Cho ES, Ahn CW, Park JS

Adrenocortical carcinomas are rare and frequently aggressive tumors that may be functional (hormone-secreting) and may cause Cushing's syndrome or virilization, or non-functional and manifest as an abdominal mass. This paper...
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A Case Report of Bilateral Adrenocortical Carcinoma Complicated by Adrenal Insufficiency

Kim MJ, Kim JH, Kim TY, Kim SW

Adrenocortical carcinoma is often functional and presents with signs and symptoms of adrenal steroid hormone excess. Adrenal insufficiency secondary to bilateral adrenocortical carcinoma is a particularly rare complication. We recently...
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A Case of Adrenocortical Carcinoma Secreting Cortisol, Androgen and Aldosterone

Choi JH, So YR, Hwang YC, Jeong IK, Ahn KJ, Chung HY, Yang SA

Primary adrenocortical carcinoma is a rare tumor, and is characterized by a peri-tumor mass effect and hormone excess signs. Adrenocortical carcinoma most commonly secretes cortisol, but tumors that secrete other...
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Unusual Presentation of Bilateral Adrenocortical Carcinoma Mimicking Adrenal Metastasis

Kim DG, Kim SD, Cha JS, Pak CH, Kim MK

A 75-year-old female visited our hospital with bilateral adrenal masses that were detected incidentally during lumbar spine magnetic resonance imaging (MRI) for the evaluation of radiating flank pain. Consecutive computed...
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Adrenocortical Carcinoma in a Patient with Congenital Adrenal Hyperplasia

Cho MS, Jin HY, Choi JH, Kim DY, Lee JJ, Yoo HW

  • KMID: 2192851
  • J Korean Soc Pediatr Endocrinol.
  • 2010 Dec;15(3):193-197.
Adrenocortical carcinoma is a very rare condition in childhood. There are only a few reports about adrenocortical carcinomas associated with congenital adrenal hyperplasia. A two-month-old male baby presented at the...
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Spontaneous Rupture of a Functioning Adrenocortical Carcinoma

Chung JO, Cho DH, Lee JH, Kwon DD, Chung DJ, Chung MY

Adrenocortical carcinoma (ACC) is a rare malignancy with poor prognosis, and it can be classified as either a functional or nonfunctional tumor. Affected patients usually present with abdominal pain or...
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The Fine Needle Aspiration Cytology of a Metastatic Pulmonary Adrenocortical Carcinoma Mimicking Primary Large Cell Carcinoma of the Lung

Kim NR, Chung DH, Lee JI, Ha SY

  • KMID: 2277569
  • Korean J Pathol.
  • 2010 Oct;44(5):558-563.
Adrenocortical carcinoma is a rare neoplasm and it has an invariably lethal prognosis. We report here on the fine needle aspiration cytologic findings of a solitary metastatic pulmonary adrenocortical carcinoma...
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A Case Report of an Aldosterone-producing Adrenocortical Carcinoma

Lee YH, Park TJ, Kim HJ, Kim DJ, Lee KW, Kim MW, Kim JH, Lee TH, Chung YS

Primary aldosteronism is a syndrome characterized by hypokalemic alkalosis and hypertension. Aldosterone-producing adenomas and bilateral adrenal hyperplasia are common causes of this syndrome. An aldosterone-producing adrenocortical carcinoma is a very...
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Clinical Review of the Pediatric Primary Adrenocortical Tumors

Chai YJ, Moon SB, Jung SE, Lee SC, Park KW

  • KMID: 2328744
  • J Korean Assoc Pediatr Surg.
  • 2007 Dec;13(2):162-168.
Adrenocortical tumors are very rare in children and the clinical course is not clearly understood. The aim of this study is to review the clinical characteristics and courses of pediatric...
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Adrenocortical Carcinoma, Myxoid Variant: A Case Report

Kim B, Yoon SO, Kim DI, Kook MC, Hong EK

  • KMID: 1521621
  • Korean J Pathol.
  • 2007 Dec;41(6):430-435.
Myxoid variant of adrenal cortical carcinoma is extremely rare and there have been only 16 such cases reported in the medical literature. Here we report on a case of 43-year-old...
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A Case of Non-Functioning Huge Adrenocortical Carcinoma Extending Into Inferior Vena Cava and Right Atrium

Kim KH, Park JC, Lim SY, Sohn IS, Yun KH, Cho SH, Hong YJ, Park HW, Kim JH, Kim W, Ahn YK, Chung IJ, Jeong MH, Cho JG, Kang JC

Primary adrenocortical carcinoma (ACC) is a rare tumor and its usual sites of metastasis are the lung (71%), lymph node (68%), liver (42%), and bone (26%). However, intracaval invasion extending...
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