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Rearrangement of anaplastic lymphoma kinase (ALK) gene is the best predictor of response to crizotinib, an ALK tyrosine kinase inhibitor. However, the prevalence of the ALK fusion is low, so accurate patient identification is crucial for successful treatment using ALK inhibitors. Furthermore, most patients with lung cancer present with advanced-stage disease at the time of diagnosis, so it is important for pathologists to detect ALK-rearranged patients while effectively maximizing small biopsy or cytology specimens. In this review, we propose a guideline recommendation for ALK testing approved by the Cardiopulmonary Pathology Study Group of the Korean Society of Pathologists.

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Mutations of the epidermal growth factor receptor (EGFR) are the strongest predictive factor for response to EGFR tyrosine kinase inhibitors (TKIs), such as gefitinib and erlotinib. EGFR TKIs are approved in Korea as a first-line treatment for lung cancer patients with mutated EGFR. Rapid and accurate EGFR mutation testing is essential for patient selection and establishing targeted therapies with EGFR TKIs. Thus, a standard set of guideline recommendations for EGFR mutation testing suitable for the Korean medical community is necessary. In this article, we propose a set of guideline recommendations for EGFR mutation testing that was discussed and approved by the Cardiopulmonary Pathology Study Group of the Korean Society of Pathologists.

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• Strategic management of transthoracic needle aspirates for histological subtyping and EGFR testing in patients with peripheral lung cancer: An institutional experience
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• Ultrasonography-Guided Core Biopsy of Supraclavicular Lymph Nodes for Diagnosis of Metastasis and Identification of Epidermal Growth Factor Receptor (EGFR) Mutation in Advanced Lung Cancer
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• Simultaneous diagnostic platform of genotyping EGFR, KRAS, and ALK in 510 Korean patients with non‐small‐cell lung cancer highlights significantly higher ALK rearrangement rate in advanced stage
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• Molecular Pathology of Lung Cancer: Current Status and Future Directions
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A case of peripheral primitive neuroectodermal tumor of the small bowel mesentery with osseous component is reported. A 23-year-old man was admitted to our hospital because of acute severe abdominal pain. Abdominal computed tomography revealed a large solid and cystic, oval shaped mass, measuring 11.0×6.0 cm in the pelvic cavity. Histologically the resected lesion consisted of sheets of undifferentiated small round cells forming Homer-Wright rosettes and perivascular pseudorosettes, and showed areas of osteoid and bone formation. Immunohistochemical studies revealed that tumor cells expressed positivity against CD99 (MIC2), CD57, neuron-specific enolase, and vimentin. Fluorescence in situ hybridization study revealed Ewing sarcoma breakpoint region 1 (EWSR1) gene rearrangement on chromosome 22q12. To the authors' knowledge this is the first documentation of a peripheral neuroectodermal tumor with osteoid and bone formation of the small bowel mesentery.

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• Undifferentiated small round cell sarcomas in the retroperitoneal space in a 12-year-old female: a rare case report
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• Huge peripheral primitive neuroectodermal tumor of the small bowel mesentery at nonage: A case report and review of the literature
  Zhe Liu, Yuan-Hong Xu, Chun-Lin Ge, Jin Long, Rui-Xia Du, Ke-Jian Guo
  World Journal of Clinical Cases.2016; 4(9): 306.     CrossRef
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  LIBO PENG, LIMIN YANG, NAN WU, BO WU
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• Diagnostic Potential of CD44, CD133, and VDR in Epithelial Ovarian Tumors: Association with Histopathology Parameters
  Ljubiša Jovanović, Branka Šošić-Jurjević, Anđa Ćirković, Sandra Dragičević, Branko Filipović, Svetlana Milenković, Stefan Dugalić, Miroslava Gojnić-Dugalić, Aleksandra Nikolić
  International Journal of Molecular Sciences.2025; 26(8): 3729.     CrossRef
• Comparison of programmed death-1 (PD-1)-positive T-cells with known prognostic indicators in breast cancer
  Ankit Kaushik, Anamika Jaiswal, B Priya, Ashish Jain, Sonal Sharma
  Journal of Family Medicine and Primary Care.2025; 14(11): 4631.     CrossRef
• Constructing high-density tissue microarrays with a novel method and a self-made tissue-arraying instrument
  Ping Qin, Liu Li, Li Zhao, Piaopiao Bian, Zhongtang Xiong
  Pathology - Research and Practice.2023; 245: 154430.     CrossRef
• The correlation of PD-L1 expression in cytological and histological material of serous high-grade ovarian cancer
  Ljubiša Jovanović, Anđa Ćirković, Ljubinka Nikolić, Milena Jović, Darko Mikić, Svetlana Milenković, Radmila Janković
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  UP Hacısalihoğlu, MA Dogan
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• PD-L1 Expression in High-Grade Serous and Clear Cell Ovarian Cancer
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  Indian Journal of Gynecologic Oncology.2022;[Epub]     CrossRef
• PD-L1 Expression in Different Segments and Histological Types of Ovarian Cancer According to Lymphocytic Infiltrate
  Ljubiša Jovanović, Radmila Janković, Andja Ćirković, Milena Jović, Tijana Janjić, Slaviša Djuričić, Svetlana Milenković
  Medicina.2021; 57(12): 1309.     CrossRef
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• Peripheral nerve sheath tumor invading the nasal cavities of a 6-year-old female Pointer dog
  Alessandra Sfacteria, Laura Perillo, Francesco Macrì, Giovanni Lanteri, Claudia Rifici, Giuseppe Mazzullo
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• High Quality Tissue Miniarray Technique Using a Conventional TV/Radio Telescopic Antenna
  Mohamed A. Elkablawy, Abdulkader M. Albasri
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• Altered Expression of PTEN and Its Major Regulator MicroRNA-21 in Pulmonary Neuroendocrine Tumors
  Hyoun Wook Lee, Seung Yeon Ha, Mee Sook Roh
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  Hua Chang, Diane Peluso, Sadiq Hussain, Michail Shipitsin, Peter Blume-Jensen
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We report here a rare case of granular cell astrocytoma. A 75-year-old man was admitted to Inha University Hospital with a three-month history of language deterioration. In a magnetic resonance imaging, a 6.5 cm-sized heterogeneous enhancing mass was seen in both the frontal lobes and the anterior genu of the corpus callosum. A stereotactic biopsy was performed. The tumor was composed of large and small round cells with abundant intracytoplasmic granules. The nuclei were bland, round to oval, and often eccentrically located. The cytoplasm of the tumor cells was positive for glial fibrillary acidic protein and S-100 protein.

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• Insights from two cases of granular cell astrocytoma as an uncommon histological variant of high-grade glioma
  Hemlata Jangir, Charli Roy, Amandeep Kumar, Ajay Garg, Mehar Chand Sharma, Vaishali Suri
  Discover Neuroscience.2026;[Epub]     CrossRef
• Cytopathological findings of granular cell glioblastoma in intraoperative squash smear preparations: A case report
  Samuel López‐Muñoz, Borja Sánchez‐Cordon, Mario Taravilla‐Loma, Isabel Esteban‐Rodríguez
  Cytopathology.2025; 36(1): 85.     CrossRef
• Granular cell tumor of the brain: case report and review of literature
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  Journal of Surgical Case Reports.2023;[Epub]     CrossRef
• Granular cell astrocytoma: Case report
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  Human Pathology: Case Reports.2018; 14: 4.     CrossRef
• Unusual presentation of a granular cell astrocytoma
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  Histopathology.2013; 63(6): 883.     CrossRef

Clear cell adenocarcinoma of the urethra is a rare disease entity with an uncertain histogenesis. Here, we present a case of primary clear cell adenocarcinoma of the female urethra with its cytological findings. A 54-year-old woman presented with a painless gross hematuria lasting 3 months. On vaginal sonography, there was a sausage-like, elongated mass in the urethra, measuring 3.8×4.3 cm. The voided urine cytology revealed small clusters of rounded or papillary cells. The necrotic debris and inflammatory cells were present within some clusters of tumor cells. These tumor cells were enlarged and had abundant clear or granular cytoplasm with cytoplasmic vacuoles. The nucleus was granular and contained vesicular chromatin with prominent nucleoli. The hobnail cells and hyaline globules were also present as in a histologic section. The histologic findings were compatible with clear cell adenocarcinoma. The tumor showed distinctive cytological features. Cytologically, however, it is necessary to make a differential diagnosis from other adenocarcinoma or high-grade urothelial carcinoma.

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• Cytological and histological findings of upper tract mucinous urothelial carcinoma with clear cell component: A case report and review of literature
  Go Kobayashi, Naohiro Uraoka, Kazuhiro Sentani, Jun Shibata, Ryosuke Nobuhiro, Yoichi Saito, Daiki Taniyama, Masanori Hanamoto, Hiroyuki Nose, Naohide Oue
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• Presentación de reporte de caso: adenocarcinoma de célula clara de uretra
  Nataly González, Yuly Ramirez, Jose Szelezsán, Daniel Rojas
  Revista Urología Colombiana / Colombian Urology Journal.2018; 27(02): 191.     CrossRef
• Clear Cell Adenocarcinoma of the Urethra: Review of the Literature
  Anthony Kodzo-Grey Venyo
  International Journal of Surgical Oncology.2015; 2015: 1.     CrossRef

A 74-year-old man suffered from jejunal perforation and adhesion to sigmoid colon due to adenocarcinoma associated with intraductal papillary mucinous neoplasm (IPMN) arising in a jejunal heterotopic pancreas. The jejunal lesion showed direct extension to the sigmoid colon, which was mistaken as sigmoid colon cancer by surgeons. Malignant transformation is a rare complication of a heterotopic pancreas. About half of malignancies in reported cases were ductal adenocarcinoma arising in the stomach, and the jejunal location is extremely rare. Furthermore, IPMN is also uncommon finding in a heterotopic pancreas.

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• A case of jejunal cancer arising from ectopic pancreas
  Makoto Eizuka, Yosuke Toya, Ryo Sugimoto, Mizuki Komai, Ako Yamada, Taku Kimura, Shunichi Yanai, Naoki Yanagawa, Akira Sasaki, Takayuki Matsumoto
  Clinical Journal of Gastroenterology.2025; 18(4): 610.     CrossRef
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  World Journal of Gastrointestinal Endoscopy.2025;[Epub]     CrossRef
• Pancreatic Intraductal Papillary Mucinous Neoplasm Arising Within Heterotopic Pancreas Tissue of the Stomach
  Rinrada Worapongpaiboon, Kasenee Tiankanon, Benjamin L. Mazer, Saowanee Ngamruengphong
  ACG Case Reports Journal.2025;[Epub]     CrossRef
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  Jiro Kimura, Takehiro Okabayashi, Kenta Sui, Takahiro Murokawa, Motoyasu Tabuchi, Masaki Aida, Jun Iwata, Yasuhiro Hata
  Surgery Open Science.2022; 8: 62.     CrossRef
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  The Japanese Journal of Gastroenterological Surgery.2020; 53(4): 371.     CrossRef
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  Irina M. Cazacu, Adriana Alexandra Luzuriaga Chavez, Graciela M. Nogueras Gonzalez, Adrian Saftoiu, Manoop S. Bhutani
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  Sang Hwa Lee
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• The diagnostic challenge of suspicious or positive malignant urine cytology findings when cystoscopy findings are normal: an outpatient blue-light flexible cystoscopy may solve the problem
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