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Showing 25 to 36 of 603 entries
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Cytological Features of a Variant NUT Midline Carcinoma of the Lung Harboring the NSD3-NUT Fusion Gene: A Case Report and Literature Review.

Case reports in pathology

Kuroda S, Suzuki S, Kurita A, Muraki M, Aoshima Y, Tanioka F, Sugimura H.
PMID: 25685583
Case Rep Pathol. 2015;2015:572951. doi: 10.1155/2015/572951. Epub 2015 Jan 19.

Background. Nuclear protein in testis (NUT) midline carcinoma (NMC) is a very rare and aggressive malignancy. In more than two-thirds of these NMC cases, a fusion between NUT and BRD4 or BRD3 has been documented; other variants are rare....

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Kuroda S, Suzuki S, Kurita A, et al. Cytological Features of a Variant NUT Midline Carcinoma of the Lung Harboring the NSD3-NUT Fusion Gene: A Case Report and Literature Review. Case Rep Pathol. 2015;2015:572951doi: 10.1155/2015/572951.
Kuroda, S., Suzuki, S., Kurita, A., Muraki, M., Aoshima, Y., Tanioka, F., & Sugimura, H. (2015). Cytological Features of a Variant NUT Midline Carcinoma of the Lung Harboring the NSD3-NUT Fusion Gene: A Case Report and Literature Review. Case reports in pathology, 2015572951. https://doi.org/10.1155/2015/572951
Kuroda, Shiho, et al. "Cytological Features of a Variant NUT Midline Carcinoma of the Lung Harboring the NSD3-NUT Fusion Gene: A Case Report and Literature Review." Case reports in pathology vol. 2015 (2015): 572951. doi: https://doi.org/10.1155/2015/572951
Kuroda S, Suzuki S, Kurita A, Muraki M, Aoshima Y, Tanioka F, Sugimura H. Cytological Features of a Variant NUT Midline Carcinoma of the Lung Harboring the NSD3-NUT Fusion Gene: A Case Report and Literature Review. Case Rep Pathol. 2015;2015:572951. doi: 10.1155/2015/572951. Epub 2015 Jan 19. PMID: 25685583; PMCID: PMC4320876.
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Metachronous Bilateral Testicular Leydig-Like Tumors Leading to the Diagnosis of Congenital Adrenal Hyperplasia (Adrenogenital Syndrome).

Case reports in pathology

Vukina J, Chism DD, Sharpless JL, Raynor MC, Milowsky MI, Funkhouser WK.
PMID: 26351608
Case Rep Pathol. 2015;2015:459318. doi: 10.1155/2015/459318. Epub 2015 Aug 16.

A 33-year-old male with a history of left testis Leydig cell tumor (LCT), 3-month status after left radical orchiectomy, presented with a rapidly enlarging (0.6 cm to 3.7 cm) right testicular mass. He underwent a right radical orchiectomy, sections...

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Vukina J, Chism DD, Sharpless JL, et al. Metachronous Bilateral Testicular Leydig-Like Tumors Leading to the Diagnosis of Congenital Adrenal Hyperplasia (Adrenogenital Syndrome). Case Rep Pathol. 2015;2015:459318doi: 10.1155/2015/459318.
Vukina, J., Chism, D. D., Sharpless, J. L., Raynor, M. C., Milowsky, M. I., & Funkhouser, W. K. (2015). Metachronous Bilateral Testicular Leydig-Like Tumors Leading to the Diagnosis of Congenital Adrenal Hyperplasia (Adrenogenital Syndrome). Case reports in pathology, 2015459318. https://doi.org/10.1155/2015/459318
Vukina, Josip, et al. "Metachronous Bilateral Testicular Leydig-Like Tumors Leading to the Diagnosis of Congenital Adrenal Hyperplasia (Adrenogenital Syndrome)." Case reports in pathology vol. 2015 (2015): 459318. doi: https://doi.org/10.1155/2015/459318
Vukina J, Chism DD, Sharpless JL, Raynor MC, Milowsky MI, Funkhouser WK. Metachronous Bilateral Testicular Leydig-Like Tumors Leading to the Diagnosis of Congenital Adrenal Hyperplasia (Adrenogenital Syndrome). Case Rep Pathol. 2015;2015:459318. doi: 10.1155/2015/459318. Epub 2015 Aug 16. PMID: 26351608; PMCID: PMC4553183.
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Synchronous Fibrolamellar Hepatocellular Carcinoma and Auricular Myxoma.

Case reports in pathology

González-Cantú YM, Rodriguez-Padilla C, Tena-Suck ML, García de la Fuente A, Mejía-Bañuelos RM, Díaz Mendoza R, Quintanilla-Garza S, Batisda-Acuña Y.
PMID: 26509093
Case Rep Pathol. 2015;2015:241708. doi: 10.1155/2015/241708. Epub 2015 Oct 05.

Synchronic occurrence of benign and malignant tumors is extremely rare. Fibrolamellar hepatocellular carcinoma represents 1% to 2% of all hepatocarcinomas, while myxomas represent about half of all the cases of primary tumors of the heart. We present the case...

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González-Cantú YM, Rodriguez-Padilla C, Tena-Suck ML, et al. Synchronous Fibrolamellar Hepatocellular Carcinoma and Auricular Myxoma. Case Rep Pathol. 2015;2015:241708doi: 10.1155/2015/241708.
González-Cantú, Y. M., Rodriguez-Padilla, C., Tena-Suck, M. L., García de la Fuente, A., Mejía-Bañuelos, R. M., Díaz Mendoza, R., Quintanilla-Garza, S., & Batisda-Acuña, Y. (2015). Synchronous Fibrolamellar Hepatocellular Carcinoma and Auricular Myxoma. Case reports in pathology, 2015241708. https://doi.org/10.1155/2015/241708
González-Cantú, Yessica M, et al. "Synchronous Fibrolamellar Hepatocellular Carcinoma and Auricular Myxoma." Case reports in pathology vol. 2015 (2015): 241708. doi: https://doi.org/10.1155/2015/241708
González-Cantú YM, Rodriguez-Padilla C, Tena-Suck ML, García de la Fuente A, Mejía-Bañuelos RM, Díaz Mendoza R, Quintanilla-Garza S, Batisda-Acuña Y. Synchronous Fibrolamellar Hepatocellular Carcinoma and Auricular Myxoma. Case Rep Pathol. 2015;2015:241708. doi: 10.1155/2015/241708. Epub 2015 Oct 05. PMID: 26509093; PMCID: PMC4609791.
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Parathyroid adenoma with prominent lymphocytic infiltrate.

Case reports in pathology

Iliadis A, Koletsa T, Kostopoulos I, Karayannopoulou G.
PMID: 25810939
Case Rep Pathol. 2015;2015:705843. doi: 10.1155/2015/705843. Epub 2015 Feb 25.

Only very few previously reported cases of pronounced lymphocytic infiltration in parathyroid adenoma can be found in the English medical literature. The objective of this report is to present such a rare case and to investigate to a certain...

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Iliadis A, Koletsa T, Kostopoulos I, et al. Parathyroid adenoma with prominent lymphocytic infiltrate. Case Rep Pathol. 2015;2015:705843doi: 10.1155/2015/705843.
Iliadis, A., Koletsa, T., Kostopoulos, I., & Karayannopoulou, G. (2015). Parathyroid adenoma with prominent lymphocytic infiltrate. Case reports in pathology, 2015705843. https://doi.org/10.1155/2015/705843
Iliadis, Alexandros, et al. "Parathyroid adenoma with prominent lymphocytic infiltrate." Case reports in pathology vol. 2015 (2015): 705843. doi: https://doi.org/10.1155/2015/705843
Iliadis A, Koletsa T, Kostopoulos I, Karayannopoulou G. Parathyroid adenoma with prominent lymphocytic infiltrate. Case Rep Pathol. 2015;2015:705843. doi: 10.1155/2015/705843. Epub 2015 Feb 25. PMID: 25810939; PMCID: PMC4355821.
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Two Different Cell Populations Is an Important Clue for Diagnosis of Primary Cutaneous Adenoid Cystic Carcinoma: Immunohistochemical Study.

Case reports in pathology

Alkan BI, Bozdogan O, Karadeniz M, Bozdoğan N.
PMID: 28243477
Case Rep Pathol. 2017;2017:7949361. doi: 10.1155/2017/7949361. Epub 2017 Jan 24.

Primary cutaneous adenoid cystic carcinoma (PCACC) is a very rare malignancy. The differential diagnosis of PCACCs in pathology practice can be difficult and a group of primary and metastatic lesions, including adenoid basal cell carcinoma of the skin, should...

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Alkan BI, Bozdogan O, Karadeniz M, et al. Two Different Cell Populations Is an Important Clue for Diagnosis of Primary Cutaneous Adenoid Cystic Carcinoma: Immunohistochemical Study. Case Rep Pathol. 2017;2017:7949361doi: 10.1155/2017/7949361.
Alkan, B. I., Bozdogan, O., Karadeniz, M., & Bozdoğan, N. (2017). Two Different Cell Populations Is an Important Clue for Diagnosis of Primary Cutaneous Adenoid Cystic Carcinoma: Immunohistochemical Study. Case reports in pathology, 20177949361. https://doi.org/10.1155/2017/7949361
Alkan, Banu Ince, et al. "Two Different Cell Populations Is an Important Clue for Diagnosis of Primary Cutaneous Adenoid Cystic Carcinoma: Immunohistochemical Study." Case reports in pathology vol. 2017 (2017): 7949361. doi: https://doi.org/10.1155/2017/7949361
Alkan BI, Bozdogan O, Karadeniz M, Bozdoğan N. Two Different Cell Populations Is an Important Clue for Diagnosis of Primary Cutaneous Adenoid Cystic Carcinoma: Immunohistochemical Study. Case Rep Pathol. 2017;2017:7949361. doi: 10.1155/2017/7949361. Epub 2017 Jan 24. PMID: 28243477; PMCID: PMC5294388.
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Ameloblastic fibrosarcoma of the mandible: a case report and brief review of the literature.

Case reports in pathology

Loya-Solis A, González-Colunga KJ, Pérez-Rodríguez CM, Ramírez-Ochoa NS, Ceceñas-Falcón L, Barboza-Quintana O.
PMID: 25861504
Case Rep Pathol. 2015;2015:245026. doi: 10.1155/2015/245026. Epub 2015 Mar 10.

Ameloblastic fibrosarcoma is an uncommon odontogenic tumor composed of a benign epithelial component and a malignant ectomesenchymal component most frequently seen in the third and fourth decades of life. It mainly presents as a painful maxillary or mandibular swelling....

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Loya-Solis A, González-Colunga KJ, Pérez-Rodríguez CM, et al. Ameloblastic fibrosarcoma of the mandible: a case report and brief review of the literature. Case Rep Pathol. 2015;2015:245026doi: 10.1155/2015/245026.
Loya-Solis, A., González-Colunga, K. J., Pérez-Rodríguez, C. M., Ramírez-Ochoa, N. S., Ceceñas-Falcón, L., & Barboza-Quintana, O. (2015). Ameloblastic fibrosarcoma of the mandible: a case report and brief review of the literature. Case reports in pathology, 2015245026. https://doi.org/10.1155/2015/245026
Loya-Solis, Abelardo, et al. "Ameloblastic fibrosarcoma of the mandible: a case report and brief review of the literature." Case reports in pathology vol. 2015 (2015): 245026. doi: https://doi.org/10.1155/2015/245026
Loya-Solis A, González-Colunga KJ, Pérez-Rodríguez CM, Ramírez-Ochoa NS, Ceceñas-Falcón L, Barboza-Quintana O. Ameloblastic fibrosarcoma of the mandible: a case report and brief review of the literature. Case Rep Pathol. 2015;2015:245026. doi: 10.1155/2015/245026. Epub 2015 Mar 10. PMID: 25861504; PMCID: PMC4377457.
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Borderline Clear Cell Adenofibroma of the Ovary.

Case reports in pathology

Kleebkaow P, Aue-Aungkul A, Temtanakitpaisan A, Kietpeerakool C.
PMID: 28465851
Case Rep Pathol. 2017;2017:3860107. doi: 10.1155/2017/3860107. Epub 2017 Mar 30.

Borderline clear cell tumors are extremely rare, and few cases have been reported in the literature. Herein, we present a case of borderline clear cell adenofibroma of the ovary in a 58-year-old woman who presented with a pelvic mass...

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Kleebkaow P, Aue-Aungkul A, Temtanakitpaisan A, et al. Borderline Clear Cell Adenofibroma of the Ovary. Case Rep Pathol. 2017;2017:3860107doi: 10.1155/2017/3860107.
Kleebkaow, P., Aue-Aungkul, A., Temtanakitpaisan, A., & Kietpeerakool, C. (2017). Borderline Clear Cell Adenofibroma of the Ovary. Case reports in pathology, 20173860107. https://doi.org/10.1155/2017/3860107
Kleebkaow, Pilaiwan, et al. "Borderline Clear Cell Adenofibroma of the Ovary." Case reports in pathology vol. 2017 (2017): 3860107. doi: https://doi.org/10.1155/2017/3860107
Kleebkaow P, Aue-Aungkul A, Temtanakitpaisan A, Kietpeerakool C. Borderline Clear Cell Adenofibroma of the Ovary. Case Rep Pathol. 2017;2017:3860107. doi: 10.1155/2017/3860107. Epub 2017 Mar 30. PMID: 28465851; PMCID: PMC5390635.
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Odontogenic Cyst with Verrucous Proliferation Exhibiting Melanin Pigmentation.

Case reports in pathology

Manaktala N, Boaz K, Soni KM, Natarajan S, Ahmed J, Bhat K, Kottieth Pallam N, Lewis AJ.
PMID: 28409045
Case Rep Pathol. 2017;2017:5079460. doi: 10.1155/2017/5079460. Epub 2017 Mar 20.

Verrucous proliferation arising from odontogenic cysts is a rare entity. We report an unusual case of an infected odontogenic cyst with verrucous proliferation and melanin pigmentation in a 13-year-old male patient who presented with an intraoral swelling in relation...

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Manaktala N, Boaz K, Soni KM, et al. Odontogenic Cyst with Verrucous Proliferation Exhibiting Melanin Pigmentation. Case Rep Pathol. 2017;2017:5079460doi: 10.1155/2017/5079460.
Manaktala, N., Boaz, K., Soni, K. M., Natarajan, S., Ahmed, J., Bhat, K., Kottieth Pallam, N., & Lewis, A. J. (2017). Odontogenic Cyst with Verrucous Proliferation Exhibiting Melanin Pigmentation. Case reports in pathology, 20175079460. https://doi.org/10.1155/2017/5079460
Manaktala, Nidhi, et al. "Odontogenic Cyst with Verrucous Proliferation Exhibiting Melanin Pigmentation." Case reports in pathology vol. 2017 (2017): 5079460. doi: https://doi.org/10.1155/2017/5079460
Manaktala N, Boaz K, Soni KM, Natarajan S, Ahmed J, Bhat K, Kottieth Pallam N, Lewis AJ. Odontogenic Cyst with Verrucous Proliferation Exhibiting Melanin Pigmentation. Case Rep Pathol. 2017;2017:5079460. doi: 10.1155/2017/5079460. Epub 2017 Mar 20. PMID: 28409045; PMCID: PMC5376934.
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On a Rare Cutaneous Metastasis from a Sacrococcygeal Chordoma.

Case reports in pathology

D'Amuri A, Brunelli M, Floccari F, De Caro F, Crisman G, Sanguedolce F, Filotico M.
PMID: 28409046
Case Rep Pathol. 2017;2017:5281239. doi: 10.1155/2017/5281239. Epub 2017 Mar 19.

Chordomas are rare malignant tumors of notochordal origin and are rare locally aggressive ones with a metastatic potential. The skin rarely is seen as metastatic site. We describe a case of an adult woman with cutaneous metastasis of a...

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D'Amuri A, Brunelli M, Floccari F, et al. On a Rare Cutaneous Metastasis from a Sacrococcygeal Chordoma. Case Rep Pathol. 2017;2017:5281239doi: 10.1155/2017/5281239.
D'Amuri, A., Brunelli, M., Floccari, F., De Caro, F., Crisman, G., Sanguedolce, F., & Filotico, M. (2017). On a Rare Cutaneous Metastasis from a Sacrococcygeal Chordoma. Case reports in pathology, 20175281239. https://doi.org/10.1155/2017/5281239
D'Amuri, Alessandro, et al. "On a Rare Cutaneous Metastasis from a Sacrococcygeal Chordoma." Case reports in pathology vol. 2017 (2017): 5281239. doi: https://doi.org/10.1155/2017/5281239
D'Amuri A, Brunelli M, Floccari F, De Caro F, Crisman G, Sanguedolce F, Filotico M. On a Rare Cutaneous Metastasis from a Sacrococcygeal Chordoma. Case Rep Pathol. 2017;2017:5281239. doi: 10.1155/2017/5281239. Epub 2017 Mar 19. PMID: 28409046; PMCID: PMC5376422.
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Eccrine Spiradenoma Arising from the Breast Skin.

Case reports in pathology

Benedict MA, Ozerdem U.
PMID: 26236527
Case Rep Pathol. 2015;2015:615158. doi: 10.1155/2015/615158. Epub 2015 Jul 07.

Eccrine spiradenomas are uncommon, benign lesions, which are thought to originate from the eccrine sweat glands. They are common in young adults and are without a sex predilection. Here we report a case of eccrine spiradenoma of the breast...

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Benedict MA, Ozerdem U. Eccrine Spiradenoma Arising from the Breast Skin. Case Rep Pathol. 2015;2015:615158doi: 10.1155/2015/615158.
Benedict, M. A., & Ozerdem, U. (2015). Eccrine Spiradenoma Arising from the Breast Skin. Case reports in pathology, 2015615158. https://doi.org/10.1155/2015/615158
Benedict, Mark A, and Ozerdem, Ugur. "Eccrine Spiradenoma Arising from the Breast Skin." Case reports in pathology vol. 2015 (2015): 615158. doi: https://doi.org/10.1155/2015/615158
Benedict MA, Ozerdem U. Eccrine Spiradenoma Arising from the Breast Skin. Case Rep Pathol. 2015;2015:615158. doi: 10.1155/2015/615158. Epub 2015 Jul 07. PMID: 26236527; PMCID: PMC4508467.
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Diagnosis of thymic clear cell carcinoma by cytology.

Case reports in pathology

Lale SA, Tiscornia-Wasserman PG, Aziz M.
PMID: 24175107
Case Rep Pathol. 2013;2013:617810. doi: 10.1155/2013/617810. Epub 2013 Sep 23.

Clear cell carcinoma of the thymus is a rare tumor. Few cases of clear-cell carcinoma of thymus have been documented (Truong et al., 1990 and Wolfe III et al., 1983). All these cases were diagnosed by histopathological examination of...

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Lale SA, Tiscornia-Wasserman PG, Aziz M. Diagnosis of thymic clear cell carcinoma by cytology. Case Rep Pathol. 2013;2013:617810doi: 10.1155/2013/617810.
Lale, S. A., Tiscornia-Wasserman, P. G., & Aziz, M. (2013). Diagnosis of thymic clear cell carcinoma by cytology. Case reports in pathology, 2013617810. https://doi.org/10.1155/2013/617810
Lale, Seema A, et al. "Diagnosis of thymic clear cell carcinoma by cytology." Case reports in pathology vol. 2013 (2013): 617810. doi: https://doi.org/10.1155/2013/617810
Lale SA, Tiscornia-Wasserman PG, Aziz M. Diagnosis of thymic clear cell carcinoma by cytology. Case Rep Pathol. 2013;2013:617810. doi: 10.1155/2013/617810. Epub 2013 Sep 23. PMID: 24175107; PMCID: PMC3794649.
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Intravascular large B-cell lymphoma presenting as interstitial lung disease.

Case reports in pathology

Khojeini EV, Song JY.
PMID: 24955271
Case Rep Pathol. 2014;2014:928065. doi: 10.1155/2014/928065. Epub 2014 May 15.

Intravascular large B-cell lymphoma (IVLBL) is a rare subtype of diffuse large B-cell lymphoma that resides in the lumen of blood vessels. Patients typically present with nonspecific findings, particularly bizarre neurologic symptoms, fever, and skin lesions. A woman presented...

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Khojeini EV, Song JY. Intravascular large B-cell lymphoma presenting as interstitial lung disease. Case Rep Pathol. 2014;2014:928065doi: 10.1155/2014/928065.
Khojeini, E. V., & Song, J. Y. (2014). Intravascular large B-cell lymphoma presenting as interstitial lung disease. Case reports in pathology, 2014928065. https://doi.org/10.1155/2014/928065
Khojeini, Elham Vali, and Song, Joo Young. "Intravascular large B-cell lymphoma presenting as interstitial lung disease." Case reports in pathology vol. 2014 (2014): 928065. doi: https://doi.org/10.1155/2014/928065
Khojeini EV, Song JY. Intravascular large B-cell lymphoma presenting as interstitial lung disease. Case Rep Pathol. 2014;2014:928065. doi: 10.1155/2014/928065. Epub 2014 May 15. PMID: 24955271; PMCID: PMC4052500.
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Showing 25 to 36 of 603 entries