Journal of Pathology and Translational Medicine

Case Study

Recurrent Indeterminate Dendritic Cell Tumor of the Skin: Jin Woo Joo, Taek Chung, Yoon Ah Cho, Sang Kyum Kim; J Pathol Transl Med. 2018;52(4):243-247. Published online April 5, 2018; DOI: https://doi.org/10.4132/jptm.2018.03.27

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Indeterminate dendritic cell tumor (IDCT) is a dendritic cell tumor that displays histologic features similar to those of Langerhans cells. The origin of the indeterminate cells may represent precursors of Langerhans cells or skin dendritic cells. IDCT is extremely rare, and tumor progression and predictive factors are not well known. Here, we report a case of a 61-year-old man who presented with a papule on his back and was finally diagnosed with IDCT based on histology and immunohistochemistry. The tumor recurred three months after surgical excision.

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Simone Zanella, Emilio Berti, Arturo Bonometti
Journal of the European Academy of Dermatology and Venereology.2023; 37(8): 1559. CrossRef

Brief Case Reports

IgG4-Related Sclerosing Mesenteritis: Seok Joo Lee, Cheol Keun Park, Woo Ick Yang, Sang Kyum Kim; J Pathol Transl Med. 2016;50(4):309-311. Published online January 11, 2016; DOI: https://doi.org/10.4132/jptm.2015.12.03

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Manifestaciones toracoabdominales de las enfermedades relacionadas con la inmunoglobulina G4
M. Álvarez García, J.C. Álvarez Torices, M.J. Díez Liébana, M.R. de la Fuente Olmos
Radiología.2023; 65(2): 165. CrossRef
Thoracoabdominal manifestations of immunoglobulin G4-related disease
M. Álvarez García, J.C. Álvarez Torices, M.J. Díez Liébana, M.R. de la Fuente Olmos
Radiología (English Edition).2023; 65(2): 165. CrossRef
Systemic manifestations – do not forget the small bowel
Stefania Chetcuti Zammit, Reena Sidhu
Current Opinion in Gastroenterology.2021; 37(3): 234. CrossRef
A case of immunoglobulin G4-related sclerosing mesenteritis without other organ involvement
Masaya Kozono, Shiroh Tanoue, Kanna Kiyama, Kenichi Jikuya, Machiko Kawahira, Makoto Hinokuchi, Hiromichi Iwaya, Shiho Arima, Shinichi Hashimoto, Kiyokazu Hiwatashi, Yoshio Fukuda, Masahiko Sakoda, Michiyo Higashi, Koichi Tokushige, Akio Ido
Clinical Journal of Gastroenterology.2021; 14(5): 1411. CrossRef
Sclerosing Mesenteritis Mimicking IgG4-related Disease
Masahide Fukuda, Toru Miyake, Akiko Matsubara, Nobuyasu Ikai, Eri Tanaka, Tomo Namura, Yasuhiro Wada, Mai Noujima, Suzuko Moritani, Kazunari Murakami, Akira Andoh, Masaji Tani, Ryoji Kushima
Internal Medicine.2020; 59(4): 513. CrossRef
A rare case report of immunoglobulin G4-related sclerosing mesenteritis and review of the literature
Zhicheng Liu, Yan Jiao, Liang He, Helei Wang, Daguang Wang
Medicine.2020; 99(41): e22579. CrossRef
Calcifying fibrous tumor of the gastrointestinal tract: A clinicopathologic review and update
Donald Turbiville, Xu-Chen Zhang
World Journal of Gastroenterology.2020; 26(37): 5597. CrossRef
Immunoglobulin G4 Unrelated Idiopathic Mesenteric Sclerosis
Tae Hyung Kwon, Kwang Bum Cho, Hyun Jik Lee, Sun Young Kwon, Yoon Suk Lee
The Korean Journal of Gastroenterology.2019; 73(1): 50. CrossRef
A Case of IgG4-related Sclerosing Mesenteritis Causing Intestinal Perforation
Junich SAKAMOTO, Masahiko WATANABE
Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association).2019; 80(9): 1658. CrossRef
„Misty mesentery“
L. P. Beyer, A. Schreyer
Der Radiologe.2018; 58(1): 56. CrossRef
IgG4-Related Disease Mimicking Crohn’s Disease: A Case Report and Review of Literature
Fabiana Ciccone, Antonio Ciccone, Mirko Di Ruscio, Filippo Vernia, Gianluca Cipolloni, Gino Coletti, Giuseppe Calvisi, Giuseppe Frieri, Giovanni Latella
Digestive Diseases and Sciences.2018; 63(4): 1072. CrossRef
Mesenteric tumour deposits arising from small‐intestine neuroendocrine tumours are frequently associated with fibrosis and IgG4‐expressing plasma cells
Jordan Roberts, Raul S Gonzalez, Frank Revetta, Chanjuan Shi
Histopathology.2018; 73(5): 795. CrossRef
A Case Report of Probable Diagnosis Group of IgG4-related Sclerosing Mesenteritis
Daiki YOKOYAMA, Takayuki TAJIMA, Masaya MUKAI, Shuji UDA, Shinichiroh HIRAIWA, Takuma TAJIRI, Eiji NOMURA, Hiroyasu MAKUUCHI
Nihon Rinsho Geka Gakkai Zasshi (Journal of Japan Surgical Association).2017; 78(10): 2245. CrossRef
Serosal involvement in IgG4-related disease: report of two cases and review of the literature
Juan González-Moreno, Inés Losada-López, Cristina Gállego-Lezaun, Mercedes García-Gasalla, Cristina Gómez Bellvert, Norberto Ortego Centeno
Rheumatology International.2016; 36(7): 1033. CrossRef
IgG4-related sclerosing mesenteritis causing bowel obstruction: a case report
Atsushi Abe, Tatsuya Manabe, Nobuyoshi Takizawa, Takashi Ueki, Daisuke Yamada, Kinuko Nagayoshi, Yoshihiko Sadakari, Hayato Fujita, Shuntaro Nagai, Hidetaka Yamamoto, Yoshinao Oda, Masafumi Nakamura
Surgical Case Reports.2016;[Epub] CrossRef

Primary Cutaneous Adenoid Cystic Carcinoma Arising in Umbilicus: Seok Joo Lee, Woo Ick Yang, Sang Kyum Kim; J Pathol Transl Med. 2016;50(4):322-324. Published online January 11, 2016; DOI: https://doi.org/10.4132/jptm.2015.11.24

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Tratamiento de las neoplasias anexiales cutáneas malignas
C. Bernárdez, L. Requena
Actas Dermo-Sifiliográficas.2018; 109(1): 6. CrossRef
Treatment of Malignant Cutaneous Adnexal Neoplasms
C. Bernárdez, L. Requena
Actas Dermo-Sifiliográficas (English Edition).2018; 109(1): 6. CrossRef
Primary cutaneous cribriform apocrine carcinoma: Case report and literature review
Jiann-Der Wu, Chih-Hsuan Changchien, Kai-Sheng Liao
Indian Journal of Dermatology, Venereology and Leprology.2018; 84(5): 569. CrossRef
Primary cutaneous adenoid cystic carcinoma with MYB aberrations: report of three cases and comprehensive review of the literature
Carlos N. Prieto‐Granada, Lei Zhang, Cristina R. Antonescu, Jean M. Henneberry, Jane L. Messina
Journal of Cutaneous Pathology.2017; 44(2): 201. CrossRef

Soft Tissue Roasi-Dorfman Disease with Features of IgG4-Related Disease in a Patient with a History of Acute Myeloid Leukemia: Cheol Keun Park, Eun Kyung Kim, Ji-Ye Kim, Hayoung Woo, Mi Jang, Hyang Sook Jeong, Woo Ick Yang, Sang Kyum Kim; J Pathol Transl Med. 2016;50(3):246-249. Published online November 17, 2015; DOI: https://doi.org/10.4132/jptm.2015.10.08

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Original Article

Clinicopathologic Characteristics of Left-Sided Colon Cancers with High Microsatellite Instability.: Sang Kyum Kim, Junjeong Choi, Hyun Ki Kim, Young Nyun Park, Si Young Song, Hoguen Kim; Korean J Pathol. 2009;43(5):428-434.; DOI: https://doi.org/10.4132/KoreanJPathol.2009.43.5.428

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Abstract PDF

BACKGROUND
High microsatellite instability (MSI-H) colorectal carcinomas (CRCs) with numerous mutations in the microsatellite sequence are characterized by a right-sided preponderance, frequent peritumoral and intratumoral lymphocytic infiltration, and frequent mucin production. However, no study has correlated anatomic site and type of genetic changes with clinicopathologic changes.
METHODS
We analyzed the histopathologic features of 135 MSI-H CRCs and compared them to 140 microsatellite stable (MSS) CRCs. Histopathologic changes in MSI-H were further analyzed according to anatomic sites and genetic changes.
RESULTS
MSI-H CRCs showed previously reported clinicopathologic findings; a right-sided preponderance, an increased number of mucinous carcinomas, and peritumoral lymphoid reactions (p<0.001 for each variable). Increased serum CEA levels showed an MSS CRC preponderance (p=0.013). We further analyzed the histologic differences between right- and left-sided MSI-H tumors. We found that MSI-H CRCs on both sides had similar clinicopathologic findings, except for higher tumor stage (p=0.048) and less frequent abnormal CEA levels in left-sided MSI-H tumors (p=0.027). We found that not all clinicopathologic features were different between hereditary nonpolyposis colorectal cancers (HNPCCs) and sporadic MSI-H CRCs.
CONCLUSIONS
These findings indicate that MSI-H CRCs of the left colon have similar clinicopathologic characteristics as right-sided MSI-H CRCs. We did not find any significant clinicopathological difference between HNPCCs and sporadic MSI-H CRCs.

Citations

Citations to this article as recorded by

Fibroblast Growth Factor Receptor 1 Gene Copy Number and mRNA Expression in Primary Colorectal Cancer and Its Clinicopathologic Correlation
Yoonjin Kwak, Soo Kyung Nam, An Na Seo, Duck-Woo Kim, Sung-Bum Kang, Woo Ho Kim, Hye Seung Lee
Pathobiology.2015; 82(2): 76. CrossRef

Case Reports

Chronic Sclerosing Dacryoadenitis: Report of 2 Cases.: Ji Eun Kwon, Sang Kyum Kim, Sang Ryul Lee, Woo Ick Yang, Haeryoung Kim; Korean J Pathol. 2008;42(2):118-122.

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Abstract PDF: Chronic sclerosing dacryoadenitis is a rare and under-recognized chronic inflammatory disease of the lacrimal gland. We describe 2 patients with a localized type of chronic sclerosing dacryoadenitis. Both patients presented with a slowly growing painless mass of the eyelid mimicking a tumorous lesion. The morphologic findings of the masses excised under the clinical diagnosis of lymphoma closely recapitulate those of chronic sclerosing sialadenitis (Kuttner tumor). Immunohistochemical staining demonstrated an increased population of IgG4-positive plasma cells confirming that this disease also belongs to the spectrum of a recently described IgG4-related sclerosing disease.

Solid Variant of Mammary Adenoid Cystic Carcinoma.: Ji Eun Kwon, Yoon Hee Lee, Ju Yeon Pyo, Sang Kyum Kim, Byeong Woo Park, Woo Ick Yang; Korean J Pathol. 2007;41(6):424-426.

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Abstract PDF: Adenoid cystic carcinoma (ACC) is a rare type of breast carcinoma and this tumor makes up less than 0.1% of all mammary carcinomas; ACC is known to show a relatively favorable prognosis. Among a variety of microscopic growth patterns of mammary ACC, a solid variant is the rarest and this can cause diagnostic difficulties. We present here a case of a solid variant of mammary ACC that occurred in the right breast of a 40-year-old woman who was initially diagnosed with invasive ductal carcinoma. We discuss the histological and clinical characteristics of this case.

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