1.Superficial Epithelioma with Sebaceous Differentiation Presented as a Yellow Plaque.
Hye Jin LEE ; Ju Yun WOO ; You Won CHOI ; Hae Young CHOI ; Ji Yeon BYUN
Annals of Dermatology 2017;29(4):516-518
No abstract available.
Carcinoma*
2.A Case of Superficial Epithelioma with Sebaceous Differentiation.
Jae Kyung KIM ; Ji Su HAN ; Chong Hyun WON ; Sung Eun CHANG ; Mi Woo LEE ; Jee Ho CHOI ; Kee Chan MOON
Korean Journal of Dermatology 2012;50(5):483-484
No abstract available.
Carcinoma
3.Epithelioma Cuniculatum Arising from Striate Keratoderma.
Wook LEW ; Kwan Chul TARK ; Soo Il CHUN
Annals of Dermatology 1992;4(2):83-86
No abstract available.
Carcinoma*
4.The utility of ultrasound-guided tru-cut biopsy in the diagnosis of occult breast carcinoma presenting as ovarian malignancy with multiple metastases: A case of unknown primary
Kareen N. Reforma ; Maria Julieta V. Germar
Acta Medica Philippina 2023;57(11):92-96
This paper documents the utility of ultrasound-guided tru-cut biopsy in the diagnosis and subsequent management of a case of occult breast carcinoma presenting with multiple distant metastases in the absence of a primary breast lesion. She was initially diagnosed as primary ovarian malignancy with metastatic disease and subsequently underwent transvaginal ultrasound-guided tru-cut biopsy of the right ovarian mass. Histologic and immunohistochemical studies were consistent with a metastatic adenocarcinoma of breast origin. The patient underwent chemotherapy for primary breast carcinoma and has responded well.
Carcinoma
5.Basosquamous carcinoma of the neck
Jan Warren A. Holgado ; Joseph E. Cachuela
Philippine Journal of Otolaryngology Head and Neck Surgery 2011;26(1):46-48
Basosquamous carcinoma, a variant of basal cell carcinoma, is rather rare with an incidence of only 1 – 2% of cases. 1, 2 It has a predilection for the head and neck region (95.6%) with primary sites including the nasal, auricular and periocular area with the neck involved in only 1.1%.1 Unlike typical basal cell carcinoma, basosquamous carcinoma behaves more aggressively with a higher tendency for metastasis and recurrence. Its rarity translates to a lack of management guidelines. Because of its pattern of growth and relative aggressiveness, treatment plans must be well laid; recurrence resulting from poor planning may lead to a worse outcome and poorer prognosis.
Carcinoma
6.Hyalinizing clear cell carcinoma of the salivary gland in an elderly female: A case report supported by EWSR1 molecular studies
Ariane Marielle F. Valle ; Jose Louie D. Remotigue ; Erick Martin H. Yturralde ; Jose M. Carnate Jr.
Acta Medica Philippina 2024;58(Early Access 2024):1-4
Hyalinizing clear cell carcinoma of the salivary gland is a rare neoplasm, accounting for only less than 1% of malignancies arising from the salivary gland. It is molecularly defined by the expression of the EWSR-ATF1 fusion oncogene. To date, there has been no previous studies published yet in the Philippines regarding the existence of this tumor. In this paper, we present a case of a 70-year-old elderly female who had a 10-year history of a gradually enlarging left lateral neck mass. Histopathologic examination showed a tumor arranged of cords, nests, and trabeculae of monomorphic round cells with abundant clear to lightly eosinophilic cytoplasm surrounded by thick hyalinized collagen bundles. Immunohistochemistry and molecular studies were done which revealed a positive p63 staining, negative SMA and S100, and an EWSR1 rearrangement in Fluorescence in situ hybridization (FISH), thus, confirming the diagnosis.
Carcinoma
7.A case of adrenocortical carcinoma accompanied by secondaryaldosteronism.
Yeon Jong KIM ; Ho dong KIM ; Hyeong Shin YOON ; Jin Hyung JANG ; Hueon KIM ; Jung Kyu LIM ; Chin Deuk HUH ; Jang Shin SOHN
Journal of Korean Society of Endocrinology 1992;7(2):160-164
No abstract available.
Adrenocortical Carcinoma*
8.Recent advances in the management of hepatocellular carcinoma.
Journal of the Korean Medical Association 2013;56(11):946-947
No abstract available.
Carcinoma, Hepatocellular*
9.Small Hepatocellular Carcinoma: Pathologic Features of 39 Cases A Comparison with Large Hepatocellular Carcinoma.
Yong Il KIM ; Geon Kook LEE ; Sang Yong SONG
Korean Journal of Pathology 1992;26(2):103-116
With advance of diagnostic imaging technics, the detection rate of small hepatocellular carcinoma (HCC) has become much increased, but the questions whether the growth pattern and histologic nature of the HCC keep maintain the original gross and microscopic features with its advancement of tumor size remain still unclear. We reviewed 39 surgically resected hepatocellular carcinomas(HCCs) with a tumor size less than or equal to 3 cm in diameter(s-HCC), and their gross and microscopic features were compared with the HCCs bigger than 3 cm (i-HCC, 199 cases). Single nodular type(SN) was the most common gross type(60%) in s-HCCs, and was followed by single nodular type with perinodular extension(SNPE; 15.4%), multinodular-discrete type(10.3%) and multinodular-confluent type(5.1%). These figures contrasted to SNPE(42.2%) and SN(20.6%) in the i-HCCs. Of the 39 s-HCCs, 25 cases(64.1%) were encapsulated, and 14 cases(36%) demonstrated intratumoral fibrous septations, being contrasted to the i-HCCs in which fibrous septa formation was mord prominent but complete capsule formation was found only in 40.2% of the larger ones. Microscopically, the trabecular type was the most frequent one(53.9%), and increased with their size while the compact type transformed into trabecular one. Thirty three cases(84.6%) were associated with macronodular cirrhosis. Seropositivity for HBsAg was found in 26 cases(66.6%), and high serum alpha-fetoprotein level over 500 IU/L was found in 15 s-HCC cases(38.4%), while 53.3% in i-HCC. The above results suggest that HCCs change their pathologic features by increase of their size, and a comparison of the details with regard to the possible mechanisms involved is discussed.
Carcinoma, Hepatocellular
10.Digital Papillary Carcinoma.
Sharon LIM ; Inju CHO ; Mi Ja LEE
Korean Journal of Pathology 2014;48(6):438-441
No abstract available.
Carcinoma, Papillary*