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Showing 1 to 12 of 603 entries
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Unusual occurrence of rare lipid-rich carcinoma and conventional invasive ductal carcinoma in the one breast: case report.

Case reports in pathology

Machalekova K, Kajo K, Bencat M.
PMID: 23050179
Case Rep Pathol. 2012;2012:387045. doi: 10.1155/2012/387045. Epub 2012 Sep 20.

A 56-year-old woman noticed a palpable mass in her left breast during self-examination. Patient was admitted to our hospital and malignant bifocal tumour was diagnosed by ultrasonography, digital mammography, magnetic resonance, and core-cut biopsy. The patient underwent planned conservative...

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Machalekova K, Kajo K, Bencat M. Unusual occurrence of rare lipid-rich carcinoma and conventional invasive ductal carcinoma in the one breast: case report. Case Rep Pathol. 2012;2012:387045doi: 10.1155/2012/387045.
Machalekova, K., Kajo, K., & Bencat, M. (2012). Unusual occurrence of rare lipid-rich carcinoma and conventional invasive ductal carcinoma in the one breast: case report. Case reports in pathology, 2012387045. https://doi.org/10.1155/2012/387045
Machalekova, Katarina, et al. "Unusual occurrence of rare lipid-rich carcinoma and conventional invasive ductal carcinoma in the one breast: case report." Case reports in pathology vol. 2012 (2012): 387045. doi: https://doi.org/10.1155/2012/387045
Machalekova K, Kajo K, Bencat M. Unusual occurrence of rare lipid-rich carcinoma and conventional invasive ductal carcinoma in the one breast: case report. Case Rep Pathol. 2012;2012:387045. doi: 10.1155/2012/387045. Epub 2012 Sep 20. PMID: 23050179; PMCID: PMC3461286.
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Rhinosporidiosis: intraoperative cytological diagnosis in an unsuspected lesion.

Case reports in pathology

Bhargava S, Grover M, Maheshwari V.
PMID: 23097732
Case Rep Pathol. 2012;2012:101832. doi: 10.1155/2012/101832. Epub 2012 Oct 11.

Rhinosporidiosis is a disease endemic to South India, Sri Lanka and some areas of the African continent. The nasal lesions can sometimes be confused with nasopharyngeal malignancy. We report here a clinically unsuspected case of rhinosporidiosis, diagnosed correctly by...

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Bhargava S, Grover M, Maheshwari V. Rhinosporidiosis: intraoperative cytological diagnosis in an unsuspected lesion. Case Rep Pathol. 2012;2012:101832doi: 10.1155/2012/101832.
Bhargava, S., Grover, M., & Maheshwari, V. (2012). Rhinosporidiosis: intraoperative cytological diagnosis in an unsuspected lesion. Case reports in pathology, 2012101832. https://doi.org/10.1155/2012/101832
Bhargava, Shruti, et al. "Rhinosporidiosis: intraoperative cytological diagnosis in an unsuspected lesion." Case reports in pathology vol. 2012 (2012): 101832. doi: https://doi.org/10.1155/2012/101832
Bhargava S, Grover M, Maheshwari V. Rhinosporidiosis: intraoperative cytological diagnosis in an unsuspected lesion. Case Rep Pathol. 2012;2012:101832. doi: 10.1155/2012/101832. Epub 2012 Oct 11. PMID: 23097732; PMCID: PMC3477536.
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Diagnosis of rosai-dorfman disease in elderly female on fine needle aspiration cytology: a case report.

Case reports in pathology

Aziz M, Ray PS, Haider N, Rathore SP.
PMID: 23097734
Case Rep Pathol. 2012;2012:806130. doi: 10.1155/2012/806130. Epub 2012 Oct 14.

Rosai-Dorfman disease (RDD) is a rare benign disorder of histiocytic proliferation that usually presents with bilateral cervical lymphadenopathy in children. We describe the case of a 50-year-old lady suffering from this disease who presented with generalized lymphadenopathy and a...

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Aziz M, Ray PS, Haider N, et al. Diagnosis of rosai-dorfman disease in elderly female on fine needle aspiration cytology: a case report. Case Rep Pathol. 2012;2012:806130doi: 10.1155/2012/806130.
Aziz, M., Ray, P. S., Haider, N., & Rathore, S. P. (2012). Diagnosis of rosai-dorfman disease in elderly female on fine needle aspiration cytology: a case report. Case reports in pathology, 2012806130. https://doi.org/10.1155/2012/806130
Aziz, Meher, et al. "Diagnosis of rosai-dorfman disease in elderly female on fine needle aspiration cytology: a case report." Case reports in pathology vol. 2012 (2012): 806130. doi: https://doi.org/10.1155/2012/806130
Aziz M, Ray PS, Haider N, Rathore SP. Diagnosis of rosai-dorfman disease in elderly female on fine needle aspiration cytology: a case report. Case Rep Pathol. 2012;2012:806130. doi: 10.1155/2012/806130. Epub 2012 Oct 14. PMID: 23097734; PMCID: PMC3477537.
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Urinary Bladder Adenocarcinoma Metastatic to the Abdominal Wall: Report of a Case with Cytohistologic Correlation.

Case reports in pathology

Nath V, Baliga M.
PMID: 27006847
Case Rep Pathol. 2016;2016:8608412. doi: 10.1155/2016/8608412. Epub 2016 Feb 23.

We report a case of adenocarcinoma metastatic to the abdominal wall in a 71-year-old man with a history of primary bladder adenocarcinoma. CT-guided core biopsy was performed; imprints and histologic sections showed malignant glands lined by tumor cells with...

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Nath V, Baliga M. Urinary Bladder Adenocarcinoma Metastatic to the Abdominal Wall: Report of a Case with Cytohistologic Correlation. Case Rep Pathol. 2016;2016:8608412doi: 10.1155/2016/8608412.
Nath, V., & Baliga, M. (2016). Urinary Bladder Adenocarcinoma Metastatic to the Abdominal Wall: Report of a Case with Cytohistologic Correlation. Case reports in pathology, 20168608412. https://doi.org/10.1155/2016/8608412
Nath, Vikas, and Baliga, Mithra. "Urinary Bladder Adenocarcinoma Metastatic to the Abdominal Wall: Report of a Case with Cytohistologic Correlation." Case reports in pathology vol. 2016 (2016): 8608412. doi: https://doi.org/10.1155/2016/8608412
Nath V, Baliga M. Urinary Bladder Adenocarcinoma Metastatic to the Abdominal Wall: Report of a Case with Cytohistologic Correlation. Case Rep Pathol. 2016;2016:8608412. doi: 10.1155/2016/8608412. Epub 2016 Feb 23. PMID: 27006847; PMCID: PMC4781945.
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Solitary Fibrous Tumor of the Sigmoid Colon Masquerading as an Adnexal Neoplasm.

Case reports in pathology

Bratton L, Salloum R, Cao W, Huber AR.
PMID: 27672467
Case Rep Pathol. 2016;2016:4182026. doi: 10.1155/2016/4182026. Epub 2016 Sep 08.

Solitary fibrous tumor is a rare, benign spindle cell neoplasm that was first described in the thoracic pleura. This tumor is now known to occur at many extrapleural sites. There are established criteria for the diagnosis of malignant solitary...

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Bratton L, Salloum R, Cao W, et al. Solitary Fibrous Tumor of the Sigmoid Colon Masquerading as an Adnexal Neoplasm. Case Rep Pathol. 2016;2016:4182026doi: 10.1155/2016/4182026.
Bratton, L., Salloum, R., Cao, W., & Huber, A. R. (2016). Solitary Fibrous Tumor of the Sigmoid Colon Masquerading as an Adnexal Neoplasm. Case reports in pathology, 20164182026. https://doi.org/10.1155/2016/4182026
Bratton, Laura, et al. "Solitary Fibrous Tumor of the Sigmoid Colon Masquerading as an Adnexal Neoplasm." Case reports in pathology vol. 2016 (2016): 4182026. doi: https://doi.org/10.1155/2016/4182026
Bratton L, Salloum R, Cao W, Huber AR. Solitary Fibrous Tumor of the Sigmoid Colon Masquerading as an Adnexal Neoplasm. Case Rep Pathol. 2016;2016:4182026. doi: 10.1155/2016/4182026. Epub 2016 Sep 08. PMID: 27672467; PMCID: PMC5031870.
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Complete Resolution of Pseudomalignant Erosion in a Reflux Gastroesophageal Polyp with Proton Pump Inhibitor.

Case reports in pathology

Nakajima T, Yagi H, Baba H, Minamisaka T, Miwa S, Hayashi S, Nishida T, Hatta H, Tsuneyama K, Imura J.
PMID: 26688768
Case Rep Pathol. 2015;2015:657059. doi: 10.1155/2015/657059. Epub 2015 Nov 24.

Pseudomalignant erosion is a diagnostic pitfall for pathologists in the differential diagnosis of malignant neoplasms. Here, we present a challenging case of a biopsy specimen from the eroded head of a polyp at the esophagogastric junction. A malignant neoplasm...

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Nakajima T, Yagi H, Baba H, et al. Complete Resolution of Pseudomalignant Erosion in a Reflux Gastroesophageal Polyp with Proton Pump Inhibitor. Case Rep Pathol. 2015;2015:657059doi: 10.1155/2015/657059.
Nakajima, T., Yagi, H., Baba, H., Minamisaka, T., Miwa, S., Hayashi, S., Nishida, T., Hatta, H., Tsuneyama, K., & Imura, J. (2015). Complete Resolution of Pseudomalignant Erosion in a Reflux Gastroesophageal Polyp with Proton Pump Inhibitor. Case reports in pathology, 2015657059. https://doi.org/10.1155/2015/657059
Nakajima, Takahiko, et al. "Complete Resolution of Pseudomalignant Erosion in a Reflux Gastroesophageal Polyp with Proton Pump Inhibitor." Case reports in pathology vol. 2015 (2015): 657059. doi: https://doi.org/10.1155/2015/657059
Nakajima T, Yagi H, Baba H, Minamisaka T, Miwa S, Hayashi S, Nishida T, Hatta H, Tsuneyama K, Imura J. Complete Resolution of Pseudomalignant Erosion in a Reflux Gastroesophageal Polyp with Proton Pump Inhibitor. Case Rep Pathol. 2015;2015:657059. doi: 10.1155/2015/657059. Epub 2015 Nov 24. PMID: 26688768; PMCID: PMC4672133.
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Hepatocellular carcinoma with both fibrolamellar and classical components: an unusual morphological pattern.

Case reports in pathology

Castro-Villabón D, Barrera-Herrera LE, Rodríguez-Urrego PA, Hudacko R, Vera A, Álvarez J, Andrade R, López R.
PMID: 25815229
Case Rep Pathol. 2015;2015:609780. doi: 10.1155/2015/609780. Epub 2015 Feb 26.

Fibrolamellar carcinoma (FLC) is an uncommon form of primary liver malignancy with unique clinical, histological, and biological characteristics. It is usually seen in young adults without underlying liver disease. Histologically, it shows large cells with abundant eosinophilic cytoplasm, large...

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Castro-Villabón D, Barrera-Herrera LE, Rodríguez-Urrego PA, et al. Hepatocellular carcinoma with both fibrolamellar and classical components: an unusual morphological pattern. Case Rep Pathol. 2015;2015:609780doi: 10.1155/2015/609780.
Castro-Villabón, D., Barrera-Herrera, L. E., Rodríguez-Urrego, P. A., Hudacko, R., Vera, A., Álvarez, J., Andrade, R., & López, R. (2015). Hepatocellular carcinoma with both fibrolamellar and classical components: an unusual morphological pattern. Case reports in pathology, 2015609780. https://doi.org/10.1155/2015/609780
Castro-Villabón, Diana, et al. "Hepatocellular carcinoma with both fibrolamellar and classical components: an unusual morphological pattern." Case reports in pathology vol. 2015 (2015): 609780. doi: https://doi.org/10.1155/2015/609780
Castro-Villabón D, Barrera-Herrera LE, Rodríguez-Urrego PA, Hudacko R, Vera A, Álvarez J, Andrade R, López R. Hepatocellular carcinoma with both fibrolamellar and classical components: an unusual morphological pattern. Case Rep Pathol. 2015;2015:609780. doi: 10.1155/2015/609780. Epub 2015 Feb 26. PMID: 25815229; PMCID: PMC4357041.
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A Large Extragnathic Keratocystic Odontogenic Tumour.

Case reports in pathology

Makarla S, Bavle RM, Muniswamappa S, Narasimhamurthy S.
PMID: 26770859
Case Rep Pathol. 2015;2015:723010. doi: 10.1155/2015/723010. Epub 2015 Dec 06.

Odontogenic keratocysts (OKCs) are developmental cysts which occur typically in the jawbones. They present more commonly in the posterior mandible of young adults than the maxilla. OKCs have been reclassified under odontogenic tumours in 2005 by the WHO and...

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Makarla S, Bavle RM, Muniswamappa S, et al. A Large Extragnathic Keratocystic Odontogenic Tumour. Case Rep Pathol. 2015;2015:723010doi: 10.1155/2015/723010.
Makarla, S., Bavle, R. M., Muniswamappa, S., & Narasimhamurthy, S. (2015). A Large Extragnathic Keratocystic Odontogenic Tumour. Case reports in pathology, 2015723010. https://doi.org/10.1155/2015/723010
Makarla, Soumya, et al. "A Large Extragnathic Keratocystic Odontogenic Tumour." Case reports in pathology vol. 2015 (2015): 723010. doi: https://doi.org/10.1155/2015/723010
Makarla S, Bavle RM, Muniswamappa S, Narasimhamurthy S. A Large Extragnathic Keratocystic Odontogenic Tumour. Case Rep Pathol. 2015;2015:723010. doi: 10.1155/2015/723010. Epub 2015 Dec 06. PMID: 26770859; PMCID: PMC4684858.
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Diffuse Neuroendocrine Cell Hyperplasia: Report of Two Cases.

Case reports in pathology

Cansız Ersöz C, Cangır AK, Dizbay Sak S.
PMID: 27293939
Case Rep Pathol. 2016;2016:3419725. doi: 10.1155/2016/3419725. Epub 2016 May 17.

Diffuse idiopathic pulmonary neuroendocrine cell hyperplasia (DIPNECH) is a rare pulmonary disorder characterised by a proliferation of neuroendocrine cells within the lung. It is believed that a minority of the patients with DIPNECH can develop carcinoid tumors. Here, we...

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Cansız Ersöz C, Cangır AK, Dizbay Sak S. Diffuse Neuroendocrine Cell Hyperplasia: Report of Two Cases. Case Rep Pathol. 2016;2016:3419725doi: 10.1155/2016/3419725.
Cansız Ersöz, C., Cangır, A. K., & Dizbay Sak, S. (2016). Diffuse Neuroendocrine Cell Hyperplasia: Report of Two Cases. Case reports in pathology, 20163419725. https://doi.org/10.1155/2016/3419725
Cansız Ersöz, Cevriye, et al. "Diffuse Neuroendocrine Cell Hyperplasia: Report of Two Cases." Case reports in pathology vol. 2016 (2016): 3419725. doi: https://doi.org/10.1155/2016/3419725
Cansız Ersöz C, Cangır AK, Dizbay Sak S. Diffuse Neuroendocrine Cell Hyperplasia: Report of Two Cases. Case Rep Pathol. 2016;2016:3419725. doi: 10.1155/2016/3419725. Epub 2016 May 17. PMID: 27293939; PMCID: PMC4886088.
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Posterior Mediastinal Adenomatoid Tumor: A Case Report and Review of the Literature.

Case reports in pathology

Parekh V, Winokur T, Cerfolio RJ, Stevens TM.
PMID: 27293940
Case Rep Pathol. 2016;2016:6898526. doi: 10.1155/2016/6898526. Epub 2016 May 08.

Adenomatoid tumor is an uncommon benign neoplasm of mesothelial differentiation that distinctively arises in and around the genital organs. In rare instances, it has been described in extragenital locations. There have been only two reports documenting its occurrence in...

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Parekh V, Winokur T, Cerfolio RJ, et al. Posterior Mediastinal Adenomatoid Tumor: A Case Report and Review of the Literature. Case Rep Pathol. 2016;2016:6898526doi: 10.1155/2016/6898526.
Parekh, V., Winokur, T., Cerfolio, R. J., & Stevens, T. M. (2016). Posterior Mediastinal Adenomatoid Tumor: A Case Report and Review of the Literature. Case reports in pathology, 20166898526. https://doi.org/10.1155/2016/6898526
Parekh, Vishwas, et al. "Posterior Mediastinal Adenomatoid Tumor: A Case Report and Review of the Literature." Case reports in pathology vol. 2016 (2016): 6898526. doi: https://doi.org/10.1155/2016/6898526
Parekh V, Winokur T, Cerfolio RJ, Stevens TM. Posterior Mediastinal Adenomatoid Tumor: A Case Report and Review of the Literature. Case Rep Pathol. 2016;2016:6898526. doi: 10.1155/2016/6898526. Epub 2016 May 08. PMID: 27293940; PMCID: PMC4875993.
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A Biphasic Pleural Tumor with Features of an Epithelioid and Small Cell Mesothelioma: Morphologic and Molecular Findings.

Case reports in pathology

Hackman S, Hammer RD, Layfield L.
PMID: 27403364
Case Rep Pathol. 2016;2016:1532424. doi: 10.1155/2016/1532424. Epub 2016 Jun 15.

Malignant mesotheliomas are generally classified into epithelioid, sarcomatoid, desmoplastic, and biphasic types with rare reports of a small cell form. These small cell variants display some morphologic overlap with desmoplastic small round cell tumors (DSRCTs) which generally occur within...

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Hackman S, Hammer RD, Layfield L. A Biphasic Pleural Tumor with Features of an Epithelioid and Small Cell Mesothelioma: Morphologic and Molecular Findings. Case Rep Pathol. 2016;2016:1532424doi: 10.1155/2016/1532424.
Hackman, S., Hammer, R. D., & Layfield, L. (2016). A Biphasic Pleural Tumor with Features of an Epithelioid and Small Cell Mesothelioma: Morphologic and Molecular Findings. Case reports in pathology, 20161532424. https://doi.org/10.1155/2016/1532424
Hackman, Sarah, et al. "A Biphasic Pleural Tumor with Features of an Epithelioid and Small Cell Mesothelioma: Morphologic and Molecular Findings." Case reports in pathology vol. 2016 (2016): 1532424. doi: https://doi.org/10.1155/2016/1532424
Hackman S, Hammer RD, Layfield L. A Biphasic Pleural Tumor with Features of an Epithelioid and Small Cell Mesothelioma: Morphologic and Molecular Findings. Case Rep Pathol. 2016;2016:1532424. doi: 10.1155/2016/1532424. Epub 2016 Jun 15. PMID: 27403364; PMCID: PMC4925982.
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Cystic and Papillary Neoplasm at the Hepatic Hilum Possibly Originating in the Peribiliary Glands.

Case reports in pathology

Miyata T, Uesaka K, Nakanuma Y.
PMID: 27656307
Case Rep Pathol. 2016;2016:9130754. doi: 10.1155/2016/9130754. Epub 2016 Aug 31.

Cystic neoplasms of the liver are divided into two types: mucinous cystic neoplasm and cystic intraductal papillary neoplasm of the bile duct. We herein report two cases of cystic and papillary neoplasm of the liver which differed from the...

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Miyata T, Uesaka K, Nakanuma Y. Cystic and Papillary Neoplasm at the Hepatic Hilum Possibly Originating in the Peribiliary Glands. Case Rep Pathol. 2016;2016:9130754doi: 10.1155/2016/9130754.
Miyata, T., Uesaka, K., & Nakanuma, Y. (2016). Cystic and Papillary Neoplasm at the Hepatic Hilum Possibly Originating in the Peribiliary Glands. Case reports in pathology, 20169130754. https://doi.org/10.1155/2016/9130754
Miyata, Takashi, et al. "Cystic and Papillary Neoplasm at the Hepatic Hilum Possibly Originating in the Peribiliary Glands." Case reports in pathology vol. 2016 (2016): 9130754. doi: https://doi.org/10.1155/2016/9130754
Miyata T, Uesaka K, Nakanuma Y. Cystic and Papillary Neoplasm at the Hepatic Hilum Possibly Originating in the Peribiliary Glands. Case Rep Pathol. 2016;2016:9130754. doi: 10.1155/2016/9130754. Epub 2016 Aug 31. PMID: 27656307; PMCID: PMC5021872.
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Showing 1 to 12 of 603 entries