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Articles de revues sur le sujet « Mixed Tumour »

Auteur : Grafiati

Publié le 7 juin 2025

Mis à jour le 2 août 2025

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1

Hellquist, Henrik, and Leslie Michaels. "Malignant mixed tumour." Virchows Archiv A Pathological Anatomy and Histopathology 409, no. 1 (1986): 93–103. http://dx.doi.org/10.1007/bf00705409.

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Thomas, M. R., K. Ward, M. Al-Khabori, and B. Natarajan. "Oncocytic mixed nasal tumour." Journal of Laryngology & Otology 107, no. 8 (1993): 732–34. http://dx.doi.org/10.1017/s0022215100124272.

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Sultana, Mst Atia, Kh Shahnewaj, Md Saiful Islam, Masuma Khatun, Nure Saba Rahman, and Mousumi Akter. "Mixed Mullerian Tumour (Carcinosarcoma) - A Rare Cervical Tumour." KYAMC Journal 7, no. 2 (2017): 818–20. http://dx.doi.org/10.3329/kyamcj.v7i2.33846.

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We report a 70 years old postmenopausal lady Mrs Johura Begum presented to us with the complaints of watery and foul smelling per vaginal discharge for 4-5 months, occasional per vaginal bleeding for 2-3 months lower abdominal pain for 15 days, fever for 7 days. On general examination she was restless, her temperature was 1020F and lower abdomen was tender. On per vaginal examination there were foul smelling discharge and a large ulcerated and necrossed mass in the vaginal canal that bleeds on touch. She was managed surgically. Now she is on chemotherapy and well.KYAMC Journal Vol. 7, No.-2, J

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Sviracevic, Branko, Srdjan Sedlar, Dragan Malobabic, and Dragomir Cuk. "Mixed malignant germ cell tumor of ovary." Medical review 64, no. 1-2 (2011): 93–95. http://dx.doi.org/10.2298/mpns1102093s.

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Introduction. Malignant tumours of ovary germ epithelium are very rare and account for about 2-5% of all ovarian tumours of germ origin. In adolescent patients under 20 years of age diagnosed to have ovarian tumour, these tumours originate from germ cells in about 70% of cases. Depending on the stage of the disease, medical treatment and age, the death rate ranges from 25% to 84%. A special group of germ tumours are mixed germ cells tumours built of two or more different types of germ tumours. Case report. This paper gives a diagnostic-therapeutic procedure and the clinical picture with the co

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FUKUNAGA, M., Y. ENDO, E. ISHIKAWA, and S. USHIGOME. "Mixed tumour of the vagina." Histopathology 28, no. 5 (1996): 457–61. http://dx.doi.org/10.1046/j.1365-2559.1996.331373.x.

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Farhat, Farhat, Rizalina A. Asnir, Ashri Yudhistira, Elvita Rahmi Daulay, and Irwan Pernandi Sagala. "An Uncommon Occurrence of Pleomorphic Adenoma in the Submandibular Salivary Gland: A Case Report." Open Access Macedonian Journal of Medical Sciences 6, no. 6 (2018): 1101–3. http://dx.doi.org/10.3889/oamjms.2018.248.

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BACKGROUND: Pleomorphic adenoma is a salivary gland tumour and mostly found in the parotid gland and quite uncommon in the submandibular gland. Pleomorphic tumours are a mixed tumour (benign mixed tumour) consisted of epithelium, myoepithelium, and mesenchyme and made of a view component variation of it.CASE REPORT: We reported a fifty-three years old man with pleomorphic adenoma that has been complaining swelling on the left neck for the last twenty years and treated with surgical excision. Computed tomography of the neck showed soft tissue tumour in the left submandibular.CONCLUSIONS: The be

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Pratama, Eka Putra, and Suly Auline Rusminan. "Gastric Neuroendocrine Neoplasm : WHO Classification 2019." Jurnal RSMH Palembang 1, no. 2 (2020): 46–62. http://dx.doi.org/10.37275/jrp.v1i2.7.

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A B S T R A C TNeuroendocrine neoplasm (NEN) of gastric is a term that includes all tumour types withneuroendocrine differentiation of gastric, well differentiated or poorly differentiatedtumour. NEN is a new term in 2019 World Health Organization (WHO) classification ofdigestive system tumours. In WHO 2019 had many updates, one of them isneuroendocrine tumours (NET) grade 3 have been included in tumour category of welldifferentiated tumour or NET. Previously, NET G3 in WHO 2010 are included as poorlydifferentiated tumour or neuroendocrine carcinoma (NEC). This neoplasm is geneticallywell diff

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Kaur, S., V. K. Bodal, M. S. Bal, R. Bhagat, and N. Gupta. "Malignant Mixed Germ Cell Ovarian Tumor in Pregnant Female." International Journal of Medical and Dental Sciences 2, no. 2 (2013): 233. http://dx.doi.org/10.19056/ijmdsjssmes/2013/v2i2/86794.

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Ovarian germ cell tumours comprise approximately 15% to 20% of all ovarian neoplasms. In pregnant females, its incidence is very low. They arise from primordial germ cells derived from the embryonal gonad. Malignant germ cell tumours comprise less than 5% of all ovarian neoplasms. Most malignant ovarian neoplasms in pregnant women are at early stages and are associated with good prognosis both for the mother and for the neonate. Histologic subtypes and prognosis do not differ from tumors not associated with pregnancy. Careful initial surgery with adequate staging biopsies followed by combinati

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Al-Khayal, Abdullah, Yasser Noureldin, Mohammad Alghafees, et al. "A decade in focus: mixed germ cell tumors with choriocarcinoma components." Annals of Medicine & Surgery 85, no. 11 (2023): 5355–58. http://dx.doi.org/10.1097/ms9.0000000000001314.

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Introduction: This 10-year registry review aimed to investigate the clinical behaviour and outcomes of mixed germ cell tumours with choriocarcinoma components, a rare and aggressive subtype of testicular cancer, in Saudi Arabia. The study explores the demographic characteristics of affected patients, tumour profiles, and the mortality rate associated with this malignancy. Methods: Utilizing data from the Saudi Cancer Registry, the authors identified 33 cases of mixed germ cell tumours with choriocarcinoma components among 1001 testicular cancer cases recorded between 2008 and 2017. Demographic

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Chmelenský, Tomáš, Pavel Hanek, Karel Franěk, Josef Rejlek, and Jiří Zvěřina. "Mixed tumour of a solitary kidney." Urologie pro praxi 17, no. 3 (2016): 129–30. http://dx.doi.org/10.36290/uro.2016.033.

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González, Mª TM, J. Del Boz González, and AS Trelles. "Apocrine mixed tumour with extensive ossification." Journal of the European Academy of Dermatology and Venereology 22, no. 1 (2007): 105–6. http://dx.doi.org/10.1111/j.1468-3083.2007.02235.x.

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Winston, Karin, and Robert Stein. "Mixed germ cell tumour after testotoxicosis." Clinical Endocrinology 81, no. 5 (2014): 786–87. http://dx.doi.org/10.1111/cen.12416.

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Hwei-Choo, Soh, Peter Russell, and Christopher Dalrymple. "Benign mixed tumour of the vulva." Pathology 37, no. 5 (2005): 389–92. http://dx.doi.org/10.1080/00313020500254388.

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Mendilcioglu, I., Z. Akinci, G. Ozbilim, S. Karaveli, and O. Erman. "Primary ovarian mixed type carcinoid tumour." Journal of Obstetrics and Gynaecology 19, no. 5 (1999): 561–62. http://dx.doi.org/10.1080/01443619964544.

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Heseltine, D., and M. G. Bramble. "Mixed endocrine adrenal tumour causing steatorrhoea." Gut 29, no. 6 (1988): 875–76. http://dx.doi.org/10.1136/gut.29.6.875-a.

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R., W. Suriza W. A., Junaidi A. I., Helmi N. M., and Imi Sairi A. H. "A rare primary thyroid mixed germ cell tumour: a case report." International Surgery Journal 10, no. 1 (2022): 130. http://dx.doi.org/10.18203/2349-2902.isj20223604.

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Germ cell tumours mostly occur in the gonads. Extragonadal site is rare and mainly located in the mediastinum, retroperitoneum and pineal gland. Germ cell tumour that occurs in the thyroid gland is extremely rare. We present our first description of a patient with a mixed germ cell tumour located primarily in the thyroid gland. A 35 years old gentleman presented with two months history of thyroid swelling associated with compressive symptoms. His neck ultrasound showed multinodular goiter with suspicious nodule (TR4) and FNAC revealed highly suggestive of a malignant lesion. Subsequently, the

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Burt, A. D., J. MacGuire, G. B. Lindop, and M. K. Browne. "Mixed Follicular-Parafollicular Carcinoma of the Thyroid." Scottish Medical Journal 32, no. 2 (1987): 50–51. http://dx.doi.org/10.1177/003693308703200209.

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We present a case of mixed follicular-parafollicular carcinoma of the thyroid. Immunohistochemical studies demonstrated the presence of both thyroglobulin and calcitonin within tumour cells. The recognition of thyroid tumours showing this mixed differentiation may have implications for existing concepts of C-cell and follicular cell development in the human thyroid.

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Talmi, Yoav P., Marisa Halpern, Yehuda Finkelstein, Rivkah Gal, and Yuval Zohar. "True malignant mixed tumour of the parotid gland." Journal of Laryngology & Otology 104, no. 4 (1990): 360–61. http://dx.doi.org/10.1017/s0022215100112721.

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AbstractCarcinoma ex-pleomorphic adenoma is an uncommon tumour of the parotid gland. True malignant mixed tumours of the parotid are rare and we could find only 14 such cases reported. A case of a 76-year-old man diagnosed as suffering from this entity is presented. The diagnosis was based on a series of immunohistochemical studies demonstrating the existence of two separate sarcomatous and carcinomatous elements. The clinical and histological data are presented and the literature is reviewed.

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E., Rajesh Goud, Manideep B., Malyadri Paladugu, and Somnath Gupta. "A rare case of minor salivary gland tumor presenting as parapharyngeal tumor." International Journal of Otorhinolaryngology and Head and Neck Surgery 11, no. 3 (2025): 316–19. https://doi.org/10.18203/issn.2454-5929.ijohns20251522.

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Parapharyngeal space tumours (PPS) are benign, uncommon located in the head and neck region. Pleomorphic adenoma the most prevalent type of salivary gland tumour can develop from the salivary glands or start in the deep lobe of the parotid gland and spread into PPS. A 59-year-old male presented with complaints of dysphagia, voice change and swelling in the soft palate. PPS tumour was detected with endoscopy, biopsy confirmed it as salivary gland tumour and PET-CT scan findings revealed a large hyper metabolic solid soft tissue density lesion in left parapharyngeal space with local extent. Tumo

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EL Filali M.D, Amal, Loubna Slama M.D, Hafsa Taheri, Hanane Saadi, and Ahmed Mimouni. "PRIMARY OVARIAN MALIGNANT MIXED MULLERIAN TUMOUR: A CASE REPORT." International Journal of Advanced Research 12, no. 05 (2024): 632–38. http://dx.doi.org/10.21474/ijar01/18764.

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Introduction:Malignant Mixed Mullerian Tumour of the Ovary (OMMMT), also known as carcinosarcoma, is a very rare tumor that represents less than 1% of all ovarian cancers. Because of its rarity, its course and treatment remain controversial Importance:It is an aggressive tumor often discovered at an advanced stage, with a double carcinomatous and sarcomatous component that affects the ovary, the main prognostic factor being the stage of the disease Current data in the literature are still limited to small case series and case reports and treatment consists of cytoreduction surgery followed by

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NATHER, A., and I. H. SUTHERLAND. "Malignant Transformation of a Benign Cutaneous Mixed Tumour." Journal of Hand Surgery 11, no. 1 (1986): 139–43. http://dx.doi.org/10.1016/0266-7681_86_90039-2.

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Whilst benign cutaneous mixed tumour is common, malignant cutaneous mixed tumour is rare. There are only eleven accepted cases of the malignant counterpart in the literature. In none was there residual benign tumour tissue present to suggest that they arose from malignant transformation of the benign tumour. We report a very rare case of a malignant transformation of a benign cutaneous mixed tumour in an eighty-four year old female. Other unusual features in this case included considerable involvement of bone in the primary lesion and the histological picture of extreme pleomorphism and active

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Moisejenko-Goluboviča, Jeļena, Oļegs Volkovs, Anna Ivanova, Eva Petrošina, and Valērija Groma. "What We Need to Learn When Exploring the Mixed Basal Cell Carcinoma of Head and Neck." Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences. 75, no. 2 (2021): 75–85. http://dx.doi.org/10.2478/prolas-2021-0013.

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Abstract Coexistence of different histopathological types of basal cell carcinomas (BCC) in the same anatomical localisation is rare, and, therefore, is engaging for histopathologists and clinicians. In many cases, the determination of a neoplasm type remains difficult, since BCC may consist of more than one histopathological subtype. Mixed BCCs often present with an aggressive course and recurrence when compared to other subtypes of a tumour. Furthermore, tumours of this type are associated with time-consuming treatment and not a very satisfactory cosmetic result, thus worsening the quality o

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Reekhaye, A., A. Harris, S. Nagarajan, and D. Chadwick. "A giant testicular mixed germ cell tumour." Annals of The Royal College of Surgeons of England 98, no. 8 (2016): e171-e172. http://dx.doi.org/10.1308/rcsann.2016.0219.

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We present a case that we believe to be the largest mixed germ cell testicular tumour reported in the United Kingdom. A 23-year-old male was admitted to our urology department with a large scrotal swelling. The patient was found to have a giant left testicular tumour and a solitary lung metastasis at presentation. He underwent an emergency radical orchidectomy and subsequently received four cycles of bleomycin, etoposide and cisplatin chemotherapy. Four months after starting treatment, the tumour markers had normalised and a repeat staging computed tomography showed no active disease. The tumo

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Hayati, Firdaus, Nurayub Mohd Ali, Levin Kesu Belani, Nornazirah Azizan, Andee Dzulkarnaen Zakaria, and Mohd Ramzisham Abdul Rahman. "Giant Mediastinal Germ Cell Tumour: An Enigma of Surgical Consideration." Case Reports in Surgery 2016 (2016): 1–5. http://dx.doi.org/10.1155/2016/7615029.

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We present a case of 16-year-old male, who was referred from private centre for dyspnoea, fatigue, and orthopnea. The chest radiograph revealed complete opacification of left chest which was confirmed by computed tomography as a large left mediastinal mass measuring 14 × 15 × 18 cm. The diagnostic needle core biopsy revealed mixed germ cell tumour with possible combination of embryonal carcinoma, yolk sac, and teratoma. After 4 cycles of neoadjuvant BEP regime, there was initial response of tumour markers but not tumour bulk. Instead of classic median sternotomy or clamshell incision, posterol

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Madi, Medhini, Supriya Bhat, Pushparaja Shetty, Ananya Madiyal, and Subhas Babu. "Benign mixed tumour of the minor salivary gland." Acta stomatologica Naissi 39, no. 87 (2023): 2618–23. http://dx.doi.org/10.5937/asn2387619m.

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Introduction: The most common major salivary gland neoplasm is the Pleomorphic adenoma. Only 10% of the pleomorphic adenoma occur in minor salivary glands. 42.8% to 68.8% of cases with intraoral lesion occurs in the palate. Here we present a rare case of a pleomorphic adenoma masquerading as a lesion of odontogenic origin. Case report presents a male patient who reported with a chief complaint of swelling in the upper left tooth region since 3 months. Panoramic radiograph revealed shadow of a soft tissue swelling in the left maxillary posterior region with destruction and resorption of the alv

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Fiaschetti, Valeria, Roberto Fiori, Eleonora Gaspari, Sonia Crusco, and Giovanni Simonetti. "Mixed Hepatoblastoma in a Young Male Adult: A Case Report and Literature Review." Case Reports in Medicine 2010 (2010): 1–5. http://dx.doi.org/10.1155/2010/919457.

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Hepatoblastoma (HB) is a rare malignant tumour of the liver and usually occurs in the first three years of life. Most of these tumours arise in the embryo; hence it seems to be unusual that hepatoblastoma occurs in adults and is an exceptional cause of primary malignant liver tumour in adult patients. The diagnosis is often overlooked, and patients might be diagnosed at late stages of the disease at risk of increased mortality. In this paper we report a case of a 30-year-old man with mixed hepatoblastoma and abdominal pain, hepatomegaly and fever. The patient under went noninvasive diagnostic

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Kadhim, Mohammad Murad Kasim, Marie Louise Jespersen, Hans Kristian Pilegaard, Marianne Nordsmark, and Gerda Elisabeth Villadsen. "Mixed Adenoneuroendocrine Carcinoma Is a Rare but Important Tumour Found in the Oesophagus." Case Reports in Gastrointestinal Medicine 2016 (2016): 1–3. http://dx.doi.org/10.1155/2016/9542687.

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Mixed adenoneuroendocrine carcinoma (MANEC) is a rare tumour of the gastrointestinal tract that consists of a dual adenocarcinomatous and neuroendocrine differentiation, each component representing at least 30% of the tumour. We report a case of a 68-year-old man who presented with two-month history of postprandial pain and vomiting. Gastric endoscopy revealed a polypoid mass in the lower part of the oesophagus. In contrast to the majority of these tumours, this biopsy was immunohistochemically positive for chromogranin A, and synaptophysin and Ki-67 index was 50% and the tumour was diagnosed

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Peregorodiev, I. N., E. Kh Kharbediya, V. V. Bokhyan, et al. "Mixed neuroendocrine and non-neuroendocrine neoplasia (MiNEN) of the stomach." Clinical Medicine (Russian Journal) 100, no. 9-10 (2022): 470–73. http://dx.doi.org/10.30629/0023-2149-2022-100-9-10-470-473.

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From the latest WHO classification of neuroendocrine neoplasms (NENs), the term MiNENs refers to mixed neuroendocrinenon-neuroendocrine tumors. A neuroendocrine component coexists with a non-neuroendocrine one in them. They are morphologically and/or immunohistochemically validated. The non-neuroendocrine component implicates adenocarcinoma, apart from other histological subtypes of carcinomas, such as squamous cell carcinoma. The neuroendocrine component can be represented by a high-grade tumour (HGNEC) in addition to neuroendocrine cancer. Gastric NENs also have subgroups of MiNENs such as m

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Ishii, Norihiro, Kenichiro Araki, Takehiko Yokobori, et al. "Presence of Cytokeratin 19-Expressing Cholangiocarcinoma-Like Tumour in a Liver Metastatic Lesion of Rectal Neuroendocrine Tumour." Case Reports in Gastroenterology 10, no. 2 (2016): 431–39. http://dx.doi.org/10.1159/000446641.

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Introduction: Tumours with adenocarcinoma and neuroendocrine components have often been reported, although the reason underlying the dual components remains unclear. Case Presentation: A 43-year-old woman with multiple liver metastatic lesions of rectal neuroendocrine tumour underwent primary tumour resection and subsequent liver transplantation. Pathological examination indicated a cholangiocarcinoma-like tumour with gland formation, adjacent to a liver metastatic lesion of the neuroendocrine tumour. This tumour comprised atypical columnar epithelium, and stained positively for neuroendocrine

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Thesleff, P., C. Benoni, H. Martensson, A. Nilsson, F. Sundler, and B. Akesson. "A mixed endocrine adrenal tumour causing steatorrhoea." Gut 28, no. 10 (1987): 1298–301. http://dx.doi.org/10.1136/gut.28.10.1298.

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Galea, Laurence A., Kiran Manya, Shomik Sengupta, and Alison Skene. "Mixed epithelial and stromal tumour of kidney." Pathology 45 (2013): S68. http://dx.doi.org/10.1097/01.pat.0000426883.31145.91.

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Coyne, John D., and Barry O’Connor. "Mixed adenoma-endocrine tumour of the stomach." Histopathology 57, no. 3 (2010): 492–94. http://dx.doi.org/10.1111/j.1365-2559.2010.03630.x.

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Pauwels, P., P. Dal Cin, R. Roumen, H. van den Berghe, and R. Sciot. "Intramuscular mixed tumour with clonal chromosomal changes." Virchows Archiv 434, no. 2 (1999): 167–71. http://dx.doi.org/10.1007/s004280050321.

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Akter, Razia, Saria Tasnim, Kamrun Nessa, and Selina Akter Banu. "Malignant Mixed Mesodermal Tumour (MMMT) of the Ovary: An Unusual Primary Tumour." Bangladesh Journal of Obstetrics & Gynaecology 34, no. 2 (2019): 124–26. http://dx.doi.org/10.3329/bjog.v34i2.58279.

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Ovarian carcinosarcoma (Malignant Mixed Mesodermal Tumour) is rare malignant tumour with a poor prognosis. We here present a case of ovarian carcinosarcoma in a 72-yearswoman suffering from intermittent lower abdominal pain for 5 months with previous history of Total Abdominal Hysterectomy (TAH) with Unilateral Salpingo-Oophorectomy (USO) due to leiomyoma 27 years back. Explanatory laparotomy and right salpingo-oophorectomy with complete surgical staging was done at Dhaka Community Medical College Hospital. Histopathology revealed both sarcomatous and carcinomatous component. Surprisingly the

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Arsenijevic, Neda, Tatjana Kastratovic, Aleksandar Zivanovic, Janko Djuric, and Marija Sorak. "Adenosarcoma Mulleri Associated with Tamoxifen use after Breast Cancer Therapy: A Case Report." Serbian Journal of Experimental and Clinical Research 17, no. 2 (2016): 161–66. http://dx.doi.org/10.1515/sjecr-2015-0045.

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Abstract The term ‘mixed Mullerian tumour’ applies to uterine tumours composed of epithelial and mesenchymal elements of Mullerian origin. These neoplasms are classified into adenomyomas, adenofi bromas, adenosarcomas, and carcinosarcomas (malignant Mullerian mixed tumours) based on whether the epithelial and stromal elements are benign or malignant. Adenosarcomas are low-grade neoplasms classified halfway along the spectrum of mixed Mullerian tumours, with adenofi bromas at one end and carcinosarcomas (malignant Mullerian mixed tumours) at the other. Adenosarcoma is a mixed Mullerian tumour c

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Raison, Nicholas, Ursula McGovern, John Hines, and Dimitrios Volanis. "Mixed adenoneuroendocrine carcinoma of the urethra." BMJ Case Reports 12, no. 3 (2019): e227948. http://dx.doi.org/10.1136/bcr-2018-227948.

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Mixed adenoneuroendocrine carcinoma (MANEC) is a rare tumour found predominantly in the gastrointestinal tract. Comprising adenocarcinomatous and neuroendocrine components, MANEC have been reported in the bladder. We report the first case to our knowledge of a MANEC arising in the urethra. A 62-year-old woman presented with a suburethral mass. Initial excision of the mass revealed it to be a MANEC. Immunohistochemistry staining was positive for CK20 and synaptophysin associated with neuroendocrine tumours. Cross-sectional imaging ruled out metastases and the patient underwent radical urethrect

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Durga, Kharidehal, Nandam Mohan Rao, and Byna Syam Sundara Rao. "Mixed Neuroendocrine - Non-Neuroendocrine Neoplasm (MiNEN) - A Rare Heterogenous Malignancy of the Pancreas." International Journal of Research and Review 10, no. 6 (2023): 306–10. http://dx.doi.org/10.52403/ijrr.20230637.

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Introduction: Pancreatic mixed neuroendocrine non-neuroendocrine neoplasms are extremely rare tumours accounting for 0.5% of all the pancreatic malignancies and 5% of all pancreatic neuroendocrine neoplasms. These tumors are rarely diagnosed preoperatively and they have a poor prognosis. Pancreatic MiNEN is characterized by 2 malignant lesions adenocarcinoma and Neuroendocrine tumour with each constituent involving more than 30% of the tumour. We report a case of 57yr old male with dullaching abdominal pain radiating to back. CA 19-9 was mildly elevated. Other laboratory tests are within norma

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Gurung, Sushma, Sabina Karim, Sagun Thapa, and Shristi Gautam. "Extragonadal Mixed Germ Cell Tumour of the Right Scapular Region: A Case Report." Journal of Nepal Medical Association 60, no. 256 (2022): 1052–55. http://dx.doi.org/10.31729/jnma.7910.

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Extragonadal germ cell tumours are rare; to the best of our knowledge, a location in the soft tissue of the right scapular region has never been previously reported in the literature. We report a case of a 9-years-old girl who presented with swelling over the right scapular region, treated by a combination of surgery and cisplatin-based chemotherapy. Immunohistochemistry and serum tumour markers concluded it to be an extragonadal mixed germ cell tumour. Our patient had a complete response up to 2 years of follow-up. This case is being reported here due to a very rare site of presentation with

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Gupta, Brajesh. "Malignant Mixed Tumour Chondroid Syringoma of the Skin: A Case Report and Literature Review." Indian Journal of Cancer Education and Research 8, no. 1 (2020): 45–47. http://dx.doi.org/10.21088/ijcer.2321.9815.8120.7.

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Brunetti, Barbara, Luisa Vera Muscatello, Louis J. DeTolla, and Giancarlo Avallone. "Unusual Myoid Differentiation in a Canine Benign Mixed Mammary Tumour." Case Reports in Veterinary Medicine 2021 (January 23, 2021): 1–4. http://dx.doi.org/10.1155/2021/6615256.

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This report describes an unusual mesenchymal differentiation in a canine benign mixed mammary tumour. A 13-year-old crossbreed female dog was submitted to surgery to remove an inguinal mammary nodule. The tumour was composed of mammary epithelium and mesenchymal populations, not only of cartilage and bone but also of myoid cells. PTAH demonstrated cross striation of striated muscle, and immunohistochemistry highlighted striated muscle expressing desmin and calponin, and smooth muscle expressing desmin, SMA, and calponin. The tumour was diagnosed as a benign mixed tumour with leio- and rhabdomy

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Subashini V. "Pleomorphic Adenoma-a Case Report." International Journal of Orofacial Biology 7, no. 1 (2023): 1–5. http://dx.doi.org/10.56501/intjorofacbiol.v7i1.743.

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Among neoplasia of head and neck, Salivary gland tumours are rare and it comprises about less than 3%.Pleomorphic adenoma is the most common benign tumour of all salivary gland tumours, which is so called mixed tumour due its wide cyto-morphological and architectural diversity. In this case report we are presenting a case of pleomorphic adenoma of buccal mucosa in a 56 year old male patient who reported to our department with complaint of pain less swelling in the left side cheek region since two years.

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Тrushina, О. V., A. V. Romanovskaya, N. F. Khvorostukhina, and E. S. Balabanova. "Mixed ovarian germ cell tumour in a girl." Voprosy praktičeskoj pediatrii 13, no. 3 (2018): 56–60. http://dx.doi.org/10.20953/1817-7646-2018-3-56-60.

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N, Sunanda, Sudha R, and Akhila M V. "GIANT MIXED EPITHELIAL OVARIAN TUMOUR: A CASE REPORT." Journal of Evolution of Medical and Dental Sciences 3, no. 51 (2014): 12043–47. http://dx.doi.org/10.14260/jemds/2014/3590.

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V. M. Haughney, R. S. Reeve, R. J., R. "An unusual mixed tumour of the uterine cervix." Journal of Obstetrics and Gynaecology 20, no. 4 (2000): 441–42. http://dx.doi.org/10.1080/01443610050112282.

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DIJK, C. M. VAN, C. D. KOOIJMAN, and A. C. M. VAN LINDERT. "Malignant mixed Müllerian tumour of the fallopian tube." Histopathology 16, no. 3 (1990): 300–302. http://dx.doi.org/10.1111/j.1365-2559.1990.tb01120.x.

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Singh, Meeta, Shramana Mandal, A. K. Kakkar, Nita Khurana, and Ankur Garg. "Mixed corticomedullary tumour with myelolipoma: a rare coexistence." Pathology 42, no. 6 (2010): 589–91. http://dx.doi.org/10.3109/00313025.2010.508741.

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NATHER, A., and I. SUTHERLAND. "Malignant transformation of a benign cutaneous mixed tumour." Journal of Hand Surgery: Journal of the British Society for Surgery of the Hand 11, no. 1 (1986): 139–43. http://dx.doi.org/10.1016/0266-7681(86)90039-2.

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Theegarten, D., Anke Reinacher, Ulrich Graeven, and Stathis Philippou. "Mixed malignant germ cell tumour of the liver." Virchows Archiv 433, no. 1 (1998): 93–96. http://dx.doi.org/10.1007/s004280050222.

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Rosell-Díaz, Ángel Manuel, Lucia Barchino-Ortiz, Ana Pulido-Pérez, Veronica Parra-Blanco, Luis Requena, and Pedro Vilas Boas. "Dermpath & Clinic: Mixed tumour of the skin." European Journal of Dermatology 30, no. 1 (2020): 73–75. http://dx.doi.org/10.1684/ejd.2020.3733.

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Abbeerami, S., Sujatha G.P. Dr., and Shambulingappa P. Dr. "An Unusual Case Report of Pleomorphic Adenoma of Minor Salivary Glands of Palate." INTERNATIONAL JOURNAL OF PHARMACEUTICAL AND BIO-MEDICAL SCIENCE 04, no. 09 (2024): 736–38. https://doi.org/10.5281/zenodo.13759024.

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Pleomorphic adenoma is a benign salivary gland tumour that exhibits wide cytomorphologic and architectural diversity. Pleomorphic adenoma (or benign mixed tumour) is a common benign salivary gland neoplasm characterised by neoplastic proliferation of epithelial (ductal) cells along with myoepithelial components, having a malignant potentiality. This paper presents a case of pleomorphic adenoma arising from minor salivary glands of palate in a female patient along with review of literature.

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