Results 41 to 50 of about 16,521 (234)

Multiple arterial embolization from left atrial myxoma in a Maltese boy [PDF]

, 1994
Atrial myxoma is rare in adults and even rarer in children. In this article the author describes. The presentation may be with embolic, obstructive or constitutional symptoms, which may be dramatic and life-threatening.
Elliott, Martin, Vassallo Agius, Paul
core  

Myxoma of the upper lip: a case report and brief review of the literature. [PDF]

, 2023
Myxomas are rare neoplasms of mesenchymal origin, which consist of many undifferentiated stellate and spindle-shaped cells in abundant loose myxoid stroma with collagen fibers. A 74-year-old patient presented in our oral and maxillofacial department with
Hliopoulos, Michael, Tilaveridou, Sofia, Tilaveridis, Ioannis, Zarampouka, Katerina, Kalaitsidou, Ioanna, Tsavos, Ioannis, Karakostas, Panagiotis   +6 more
core   +1 more source

Intramuscular myxoma with chondroid features: two cases expanding the morphological spectrum

Histopathology, EarlyView.
Background Intramuscular myxoma is a benign mesenchymal tumour typically composed of bland spindle to stellate cells in abundant myxoid stroma and usually characterized by GNAS mutations. Chondroid matrix has not been previously reported in intramuscular myxoma.
Bethany Batson, Azfar Neyaz, Lucas Da Gama Lobo, Rana Naous, Stella J Lee, Ivy John   +5 more
wiley   +1 more source

Peripheral odontogenic myxoma of maxillary gingiva: A rare clinical entity

Journal of Indian Society of Periodontology, 2013
Odontogenic myxoma comprises 3-6% of all odontogenic tumors. Odontogenic myxomas are relatively rare benign mesenchymal tumors found exclusively in the tooth-bearing areas of the jaw and are usually located centrally in the mandible.
Vijay Kumar Jain, Soundarya Narayana Reddy   +1 more
doaj   +1 more source

Cell Therapy for Periodontal, Soft‐Tissue, and Craniofacial Regeneration

Journal of Periodontal Research, EarlyView.
The clinical translation of mesenchymal stem/stromal cells (MSCs) represents a major advancement in dentistry, especially for periodontal, soft‐tissue, and craniofacial regeneration. However, several challenges remain to be addressed, including the absence of standardised protocols, limited scalability, regulatory hurdles, a lack of well‐controlled ...
Kamal Mustafa, Shuntaro Yamada, Nerea Sanchez, Magdalena Mayol, Cecilie Gjerde, Mariano Sanz   +5 more
wiley   +1 more source

Research progress in the diagnosis and treatment of pseudomyxoma peritonei

World Journal of Surgical Oncology
Pseudomyxoma Peritonei (PMP) is a rare and complex clinical syndrome characterized by the extensive implantation and metastasis of tumor cells from different tissues within the abdominal cavity, accompanied by the continuous secretion of large amounts of
Shi Guanjun, Wang Chong, Zhang Pu, An Lubiao, Zhou Haipeng, Ma Ruiqing, Shou Huafeng   +6 more
doaj   +1 more source

Left Atrial Myxoma Mimicking Mitral Stenosis

, 2012
Cardiac myxoma is a benign (non-malignant) neoplasm that represents the most common primary tumour of the heart. We present the case of a 36 year old woman with background hypertension who presented with features of left ventricular failure and seizures,
Dike B Ojji, Zaiyad Habib, Odiase Omonua, Manmak H Mamven, Hamamatu Osaze, Karen Sliwa   +5 more
core   +1 more source

The great simulator [PDF]

, 1993
Cardiac myxoma often simulates multisystem disease and initially defies diagnosis. In this paper, we present three cases of cardiac myxoma in adults.
Mallia, Carmel, Aquilina, Oscar, Fenech, Frederick F.   +2 more
core  

Right atrial myxoma with peripheral eosinophilia: Eosinophilia in cardiac myxoma

, 2020
Background Cardiac myxoma is the most common type of primary cardiac tumors. It is known that inflammatory markers are increased in the setting of myxoma, like C‐reactive protein, erythrocyte sedimentation rate, and interleukin‐6. The association between
Mendoza, Cesar, Alejandro Pajares, Walter, Fernandes, Gilson C, Amboss, Natalia, Salerno, Tomas A   +4 more
core   +1 more source

Catastrophic Antiphospholipid Syndrome in a Young Female Complicated by Systemic Lupus Erythematosus and Left Atrial Myxoma: A Rare Case Report

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Catastrophic antiphospholipid syndrome (CAPS) is a fulminant and rare variant of antiphospholipid syndrome characterized by rapidly progressive multiorgan thrombosis and a high mortality rate. Its diagnosis is often challenging due to overlapping clinical features with sepsis, thromboembolic disorders, and systemic autoimmune diseases.
Nazmin Ahmed, Mohammad Nazrul Hossain, Abdullah Salman, Sabrina Yesmin, S. M. G. Saklayen   +4 more
wiley   +1 more source