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Showing 13 to 24 of 603 entries
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Eumycetoma Osteomyelitis of the Calcaneus in a Child: A Radiologic-Pathologic Correlation following Total Calcanectomy.

Case reports in pathology

El-Sobky TA, Haleem JF, Samir S.
PMID: 26483983
Case Rep Pathol. 2015;2015:129020. doi: 10.1155/2015/129020. Epub 2015 Sep 21.

Fungi are unusual causes of pedal osteomyelitis in children and adolescents. Eumycetoma is a chronic cutaneous and subcutaneous infection caused by various genera of fungi. A provisional diagnosis of foot mycetoma is made after clinical assessment. Radiologic-pathologic correlation is...

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El-Sobky TA, Haleem JF, Samir S. Eumycetoma Osteomyelitis of the Calcaneus in a Child: A Radiologic-Pathologic Correlation following Total Calcanectomy. Case Rep Pathol. 2015;2015:129020doi: 10.1155/2015/129020.
El-Sobky, T. A., Haleem, J. F., & Samir, S. (2015). Eumycetoma Osteomyelitis of the Calcaneus in a Child: A Radiologic-Pathologic Correlation following Total Calcanectomy. Case reports in pathology, 2015129020. https://doi.org/10.1155/2015/129020
El-Sobky, Tamer Ahmed, et al. "Eumycetoma Osteomyelitis of the Calcaneus in a Child: A Radiologic-Pathologic Correlation following Total Calcanectomy." Case reports in pathology vol. 2015 (2015): 129020. doi: https://doi.org/10.1155/2015/129020
El-Sobky TA, Haleem JF, Samir S. Eumycetoma Osteomyelitis of the Calcaneus in a Child: A Radiologic-Pathologic Correlation following Total Calcanectomy. Case Rep Pathol. 2015;2015:129020. doi: 10.1155/2015/129020. Epub 2015 Sep 21. PMID: 26483983; PMCID: PMC4592886.
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Hybrid Desmoplastic/Follicular Ameloblastoma of the Mandible: A Case Report and Review of the Literature.

Case reports in pathology

Iwase M, Fukuoka A, Tanaka Y, Saida N, Onaka E, Bando S, Kondo G.
PMID: 28584671
Case Rep Pathol. 2017;2017:7031414. doi: 10.1155/2017/7031414. Epub 2017 May 11.

Desmoplastic ameloblastoma (DA) is one of the 6 histopathological subtypes of ameloblastoma. Hybrid lesions in which histopathologically conventional ameloblastoma coexists with areas of DA are rare. A 40-year-old male was referred to our hospital complaining of a swelling in...

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Iwase M, Fukuoka A, Tanaka Y, et al. Hybrid Desmoplastic/Follicular Ameloblastoma of the Mandible: A Case Report and Review of the Literature. Case Rep Pathol. 2017;2017:7031414doi: 10.1155/2017/7031414.
Iwase, M., Fukuoka, A., Tanaka, Y., Saida, N., Onaka, E., Bando, S., & Kondo, G. (2017). Hybrid Desmoplastic/Follicular Ameloblastoma of the Mandible: A Case Report and Review of the Literature. Case reports in pathology, 20177031414. https://doi.org/10.1155/2017/7031414
Iwase, Masayasu, et al. "Hybrid Desmoplastic/Follicular Ameloblastoma of the Mandible: A Case Report and Review of the Literature." Case reports in pathology vol. 2017 (2017): 7031414. doi: https://doi.org/10.1155/2017/7031414
Iwase M, Fukuoka A, Tanaka Y, Saida N, Onaka E, Bando S, Kondo G. Hybrid Desmoplastic/Follicular Ameloblastoma of the Mandible: A Case Report and Review of the Literature. Case Rep Pathol. 2017;2017:7031414. doi: 10.1155/2017/7031414. Epub 2017 May 11. PMID: 28584671; PMCID: PMC5443997.
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Keratoacanthoma of the Nasal Septum Secondary to Ranibizumab Use.

Case reports in pathology

Cohn JE, Caruso Sales HM, Nguyen GH, Spector H, Briskin K.
PMID: 28584672
Case Rep Pathol. 2017;2017:8257590. doi: 10.1155/2017/8257590. Epub 2017 May 11.

Keratoacanthoma (KA) is a benign epithelial tumor that typically presents as a firm, cone-shaped, flesh-colored nodule with a central horn-filled crater. KA is considered to be a low-grade variant of squamous cell carcinoma (SCC). We report a rare case...

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Cohn JE, Caruso Sales HM, Nguyen GH, et al. Keratoacanthoma of the Nasal Septum Secondary to Ranibizumab Use. Case Rep Pathol. 2017;2017:8257590doi: 10.1155/2017/8257590.
Cohn, J. E., Caruso Sales, H. M., Nguyen, G. H., Spector, H., & Briskin, K. (2017). Keratoacanthoma of the Nasal Septum Secondary to Ranibizumab Use. Case reports in pathology, 20178257590. https://doi.org/10.1155/2017/8257590
Cohn, Jason E, et al. "Keratoacanthoma of the Nasal Septum Secondary to Ranibizumab Use." Case reports in pathology vol. 2017 (2017): 8257590. doi: https://doi.org/10.1155/2017/8257590
Cohn JE, Caruso Sales HM, Nguyen GH, Spector H, Briskin K. Keratoacanthoma of the Nasal Septum Secondary to Ranibizumab Use. Case Rep Pathol. 2017;2017:8257590. doi: 10.1155/2017/8257590. Epub 2017 May 11. PMID: 28584672; PMCID: PMC5443992.
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Respiratory Epithelium Lined Cyst of the Maxilla: Differential Diagnosis.

Case reports in pathology

Martinelli-Kläy CP, Chatelain S, Salvado F, Lombardi T.
PMID: 29093979
Case Rep Pathol. 2017;2017:6249649. doi: 10.1155/2017/6249649. Epub 2017 Sep 28.

Maxillary cysts, including the cysts lined by respiratory epithelium, can present a diagnostic challenge. We report an unusual case of a maxillary cyst on an endodontically treated tooth #16, in which the cavity was totally lined by a respiratory...

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Martinelli-Kläy CP, Chatelain S, Salvado F, et al. Respiratory Epithelium Lined Cyst of the Maxilla: Differential Diagnosis. Case Rep Pathol. 2017;2017:6249649doi: 10.1155/2017/6249649.
Martinelli-Kläy, C. P., Chatelain, S., Salvado, F., & Lombardi, T. (2017). Respiratory Epithelium Lined Cyst of the Maxilla: Differential Diagnosis. Case reports in pathology, 20176249649. https://doi.org/10.1155/2017/6249649
Martinelli-Kläy, C P, et al. "Respiratory Epithelium Lined Cyst of the Maxilla: Differential Diagnosis." Case reports in pathology vol. 2017 (2017): 6249649. doi: https://doi.org/10.1155/2017/6249649
Martinelli-Kläy CP, Chatelain S, Salvado F, Lombardi T. Respiratory Epithelium Lined Cyst of the Maxilla: Differential Diagnosis. Case Rep Pathol. 2017;2017:6249649. doi: 10.1155/2017/6249649. Epub 2017 Sep 28. PMID: 29093979; PMCID: PMC5637856.
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Lipomatous Hypertrophy of the Atrial Septum in a Patient Undergoing Coronary Artery Bypass Surgery.

Case reports in pathology

Strecker T, Weyand M, Agaimy A.
PMID: 28078155
Case Rep Pathol. 2016;2016:2080875. doi: 10.1155/2016/2080875. Epub 2016 Dec 19.

No abstract available.

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Strecker T, Weyand M, Agaimy A. Lipomatous Hypertrophy of the Atrial Septum in a Patient Undergoing Coronary Artery Bypass Surgery. Case Rep Pathol. 2016;2016:2080875doi: 10.1155/2016/2080875.
Strecker, T., Weyand, M., & Agaimy, A. (2016). Lipomatous Hypertrophy of the Atrial Septum in a Patient Undergoing Coronary Artery Bypass Surgery. Case reports in pathology, 20162080875. https://doi.org/10.1155/2016/2080875
Strecker, Thomas, et al. "Lipomatous Hypertrophy of the Atrial Septum in a Patient Undergoing Coronary Artery Bypass Surgery." Case reports in pathology vol. 2016 (2016): 2080875. doi: https://doi.org/10.1155/2016/2080875
Strecker T, Weyand M, Agaimy A. Lipomatous Hypertrophy of the Atrial Septum in a Patient Undergoing Coronary Artery Bypass Surgery. Case Rep Pathol. 2016;2016:2080875. doi: 10.1155/2016/2080875. Epub 2016 Dec 19. PMID: 28078155; PMCID: PMC5204074.
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Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature.

Case reports in pathology

AlAbdulsalam A, Arafah M.
PMID: 28078157
Case Rep Pathol. 2016;2016:7289017. doi: 10.1155/2016/7289017. Epub 2016 Dec 18.

Dendritic fibromyxolipoma is a rare and distinctive soft tissue neoplasm that is considered by many authors as a variant of spindle cell lipoma and characterized by the presence of dendritic cytoplasmic processes, plexiform vascular pattern, and keloidal collagen. It...

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AlAbdulsalam A, Arafah M. Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature. Case Rep Pathol. 2016;2016:7289017doi: 10.1155/2016/7289017.
AlAbdulsalam, A., & Arafah, M. (2016). Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature. Case reports in pathology, 20167289017. https://doi.org/10.1155/2016/7289017
AlAbdulsalam, Abdulrahim, and Arafah, Maha. "Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature." Case reports in pathology vol. 2016 (2016): 7289017. doi: https://doi.org/10.1155/2016/7289017
AlAbdulsalam A, Arafah M. Dendritic Fibromyxolipoma of the Pyriform Sinus: A Case Report and Review of the Literature. Case Rep Pathol. 2016;2016:7289017. doi: 10.1155/2016/7289017. Epub 2016 Dec 18. PMID: 28078157; PMCID: PMC5203870.
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A case of unsuspected peritoneal mesothelioma occurring with colonic adenocarcinoma masquerading as peritoneal metastases.

Case reports in pathology

Xie W, Green LK, Patel RA, Lai S.
PMID: 24963429
Case Rep Pathol. 2014;2014:838506. doi: 10.1155/2014/838506. Epub 2014 May 20.

We report a case of synchronous primary colonic adenocarcinoma and malignant mesothelioma. A 61-year-old male presented with a six-month history of fatigue and weight loss. An abdominal computed tomography (CT) scan showed a 5.8 cm partially obstructing mass in...

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Xie W, Green LK, Patel RA, et al. A case of unsuspected peritoneal mesothelioma occurring with colonic adenocarcinoma masquerading as peritoneal metastases. Case Rep Pathol. 2014;2014:838506doi: 10.1155/2014/838506.
Xie, W., Green, L. K., Patel, R. A., & Lai, S. (2014). A case of unsuspected peritoneal mesothelioma occurring with colonic adenocarcinoma masquerading as peritoneal metastases. Case reports in pathology, 2014838506. https://doi.org/10.1155/2014/838506
Xie, Wei, et al. "A case of unsuspected peritoneal mesothelioma occurring with colonic adenocarcinoma masquerading as peritoneal metastases." Case reports in pathology vol. 2014 (2014): 838506. doi: https://doi.org/10.1155/2014/838506
Xie W, Green LK, Patel RA, Lai S. A case of unsuspected peritoneal mesothelioma occurring with colonic adenocarcinoma masquerading as peritoneal metastases. Case Rep Pathol. 2014;2014:838506. doi: 10.1155/2014/838506. Epub 2014 May 20. PMID: 24963429; PMCID: PMC4055023.
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Oral verruciform xanthoma: a case report and literature review.

Case reports in pathology

Marques YM, de Andrade CR, Machado de Sousa SC, Navarro CM.
PMID: 25548705
Case Rep Pathol. 2014;2014:641015. doi: 10.1155/2014/641015. Epub 2014 Dec 08.

Oral verruciform xanthoma represents an uncommon entity, which affects mainly oral mucosa. This paper presents the major clinical and histological features of oral verruciform xanthoma and reports a case on the tongue. The differential diagnosis and a literature review...

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Marques YM, de Andrade CR, Machado de Sousa SC, et al. Oral verruciform xanthoma: a case report and literature review. Case Rep Pathol. 2014;2014:641015doi: 10.1155/2014/641015.
Marques, Y. M., de Andrade, C. R., Machado de Sousa, S. C., & Navarro, C. M. (2014). Oral verruciform xanthoma: a case report and literature review. Case reports in pathology, 2014641015. https://doi.org/10.1155/2014/641015
Marques, Yonara Maria Freire Soares, et al. "Oral verruciform xanthoma: a case report and literature review." Case reports in pathology vol. 2014 (2014): 641015. doi: https://doi.org/10.1155/2014/641015
Marques YM, de Andrade CR, Machado de Sousa SC, Navarro CM. Oral verruciform xanthoma: a case report and literature review. Case Rep Pathol. 2014;2014:641015. doi: 10.1155/2014/641015. Epub 2014 Dec 08. PMID: 25548705; PMCID: PMC4274645.
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Carcinosarcoma of the ureter with a small cell component: report of a rare pathologic entity and potential for diagnostic error on biopsy.

Case reports in pathology

Newsom K, Tojuola B, Al-Quran S, Parekattil S, Hamilton W, Vila Duckworth L.
PMID: 25587477
Case Rep Pathol. 2014;2014:391615. doi: 10.1155/2014/391615. Epub 2014 Dec 24.

Carcinosarcomas of the ureter are rare biphasic neoplasms, composed of both malignant epithelial (carcinomatous) and malignant mesenchymal (sarcomatous) components. Carcinosarcomas of the urinary tract are exceedingly rare. We report a unique case of a carcinosarcoma of the ureter with...

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Newsom K, Tojuola B, Al-Quran S, et al. Carcinosarcoma of the ureter with a small cell component: report of a rare pathologic entity and potential for diagnostic error on biopsy. Case Rep Pathol. 2014;2014:391615doi: 10.1155/2014/391615.
Newsom, K., Tojuola, B., Al-Quran, S., Parekattil, S., Hamilton, W., & Vila Duckworth, L. (2014). Carcinosarcoma of the ureter with a small cell component: report of a rare pathologic entity and potential for diagnostic error on biopsy. Case reports in pathology, 2014391615. https://doi.org/10.1155/2014/391615
Newsom, Kent, et al. "Carcinosarcoma of the ureter with a small cell component: report of a rare pathologic entity and potential for diagnostic error on biopsy." Case reports in pathology vol. 2014 (2014): 391615. doi: https://doi.org/10.1155/2014/391615
Newsom K, Tojuola B, Al-Quran S, Parekattil S, Hamilton W, Vila Duckworth L. Carcinosarcoma of the ureter with a small cell component: report of a rare pathologic entity and potential for diagnostic error on biopsy. Case Rep Pathol. 2014;2014:391615. doi: 10.1155/2014/391615. Epub 2014 Dec 24. PMID: 25587477; PMCID: PMC4284926.
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Osteoclastic giant cell rich squamous cell carcinoma of the uterine cervix: a case report and review of the literature.

Case reports in pathology

Alemán-Meza L, Gómez-Macías GS, Barboza-Quintana O, Garza-Guajardo R, Loya-Solis A.
PMID: 25587478
Case Rep Pathol. 2014;2014:415328. doi: 10.1155/2014/415328. Epub 2014 Dec 22.

Cervical carcinoma is the most common malignancy of the female genital tract and represents the second most common malignancy in women worldwide. Histologically 85 to 90% of cervical cancers are squamous cell carcinoma. Osteoclastic giant cell rich squamous cell...

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Alemán-Meza L, Gómez-Macías GS, Barboza-Quintana O, et al. Osteoclastic giant cell rich squamous cell carcinoma of the uterine cervix: a case report and review of the literature. Case Rep Pathol. 2014;2014:415328doi: 10.1155/2014/415328.
Alemán-Meza, L., Gómez-Macías, G. S., Barboza-Quintana, O., Garza-Guajardo, R., & Loya-Solis, A. (2014). Osteoclastic giant cell rich squamous cell carcinoma of the uterine cervix: a case report and review of the literature. Case reports in pathology, 2014415328. https://doi.org/10.1155/2014/415328
Alemán-Meza, Lucía, et al. "Osteoclastic giant cell rich squamous cell carcinoma of the uterine cervix: a case report and review of the literature." Case reports in pathology vol. 2014 (2014): 415328. doi: https://doi.org/10.1155/2014/415328
Alemán-Meza L, Gómez-Macías GS, Barboza-Quintana O, Garza-Guajardo R, Loya-Solis A. Osteoclastic giant cell rich squamous cell carcinoma of the uterine cervix: a case report and review of the literature. Case Rep Pathol. 2014;2014:415328. doi: 10.1155/2014/415328. Epub 2014 Dec 22. PMID: 25587478; PMCID: PMC4284984.
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Metastasis of Malignant Melanoma to Urinary Bladder: A Case Report and Review of the Literature.

Case reports in pathology

Meunier R, Pareek G, Amin A.
PMID: 26106499
Case Rep Pathol. 2015;2015:173870. doi: 10.1155/2015/173870. Epub 2015 May 28.

Aims. Metastatic malignant melanoma of the urinary bladder is a rare clinical entity, with only twenty-three published cases to date. We present a case of this rare entity, a thorough review of the literature, and differential diagnosis of melanoma...

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Meunier R, Pareek G, Amin A. Metastasis of Malignant Melanoma to Urinary Bladder: A Case Report and Review of the Literature. Case Rep Pathol. 2015;2015:173870doi: 10.1155/2015/173870.
Meunier, R., Pareek, G., & Amin, A. (2015). Metastasis of Malignant Melanoma to Urinary Bladder: A Case Report and Review of the Literature. Case reports in pathology, 2015173870. https://doi.org/10.1155/2015/173870
Meunier, Rashna, et al. "Metastasis of Malignant Melanoma to Urinary Bladder: A Case Report and Review of the Literature." Case reports in pathology vol. 2015 (2015): 173870. doi: https://doi.org/10.1155/2015/173870
Meunier R, Pareek G, Amin A. Metastasis of Malignant Melanoma to Urinary Bladder: A Case Report and Review of the Literature. Case Rep Pathol. 2015;2015:173870. doi: 10.1155/2015/173870. Epub 2015 May 28. PMID: 26106499; PMCID: PMC4464585.
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Unusual dermoid cyst in oral cavity.

Case reports in pathology

Vieira EM, Borges AH, Volpato LE, Porto AN, Carvalhosa AA, Botelho Gde A, Bandeca MC.
PMID: 24818032
Case Rep Pathol. 2014;2014:389752. doi: 10.1155/2014/389752. Epub 2014 Apr 10.

Dermoid cysts in oral cavity are unusual lesions. Their etiology is not yet clear and can be associated with trapped cells as a result of the inclusion error resulting in the development into the ectoderm, mesoderm, and endoderm tissues....

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Vieira EM, Borges AH, Volpato LE, et al. Unusual dermoid cyst in oral cavity. Case Rep Pathol. 2014;2014:389752doi: 10.1155/2014/389752.
Vieira, E. M., Borges, A. H., Volpato, L. E., Porto, A. N., Carvalhosa, A. A., Botelho, G. d. e. . A., & Bandeca, M. C. (2014). Unusual dermoid cyst in oral cavity. Case reports in pathology, 2014389752. https://doi.org/10.1155/2014/389752
Vieira, Evanice Menezes Marçal, et al. "Unusual dermoid cyst in oral cavity." Case reports in pathology vol. 2014 (2014): 389752. doi: https://doi.org/10.1155/2014/389752
Vieira EM, Borges AH, Volpato LE, Porto AN, Carvalhosa AA, Botelho Gde A, Bandeca MC. Unusual dermoid cyst in oral cavity. Case Rep Pathol. 2014;2014:389752. doi: 10.1155/2014/389752. Epub 2014 Apr 10. PMID: 24818032; PMCID: PMC4003773.
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Showing 13 to 24 of 603 entries