The authors report a case of a rare first branchial cranio facial malformation, combined with a posterieur maxilla cleft, and macrostomia. The authors insist on the clinical aspect, and the difficult classification of this malformations.
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Ribbing's disease is a rare form of sclerosing bone dysplasia characterized by exuberant yet benign endosteal bone, and periosteum formation in the diaphysis of long bones. Diagnosis relies on exclusionary criteria, as the primary clinical manifestations entail progressive pain unresponsive to analgesic therapy, accompanied by serological markers within normal ranges. Pain management constitutes the cornerstone of treatment, with surgery appearing to offer the most efficacious approach, despite the absence of a standardized therapeutic algorithm.
View Article and Find Full Text PDFThe Varied Presentations of Sinonasal Region Schwannomas: Apropos of Four Cases.
Indian J Otolaryngol Head Neck Surg
October 2022
Department of Otorhinolaryngology, Head and Neck Surgery, Medanta- The Medicity, 8th Floor, Sector-38, Gurugram, Haryana 122001 India.
Schwannomas of the sinonasal compartment are rare benign neoplasms of peripheral nerve sheath origin and constitute ~ 4% of all head and neck schwannomas. The presentation may simulate a range of benign and intermediate grade pathologies. Management involves surgical excision via open or endoscopic approach.
View Article and Find Full Text PDF[Adrenal myelolipoma, review of the literature in Mexico apropos of two cases].
Rev Med Inst Mex Seguro Soc
March 2022
Secretaría de Salud. Hospital General de México "Dr. Eduardo Liceaga", Departamento de Anatomía Patológica. Ciudad de México, México.
Background: Adrenal myelolipomas (ML) are rare benign neoplasms compound of adipose and myeloid tissue. Clinically they are usually asymptomatic, being diagnosed generally by incident. In Mexico, there are only 32 published cases of ML, these occur between 37 and 65 years, with the male-female ratio being 1:1.
View Article and Find Full Text PDFClinicopathologic and Molecular Characteristics of and Diagnostic Dilemmas in Invasive Breast Carcinoma with Choriocarcinomatous Pattern apropos a New Case: A Literature Review with New Findings.
Pathobiology
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Department of Radiology, Incheon St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Incheon, Republic of Korea.
Article Synopsis
- IBC-CP (Invasive Breast Carcinoma with Choriocarcinomatous Pattern) is a rare form of breast cancer marked by specific cell arrangements and β-hCG expression, making it hard to differentiate from metastatic choriocarcinoma.
- A study analyzed clinicopathologic differences between 17 IBC-CP patients and 8 metastatic choriocarcinoma patients, finding older age and fewer histories of reproductive issues in IBC-CP patients.
- Genetic analysis revealed a TP53 mutation in both cancer types and indicated that the loss of the PTEN gene could be linked to the choriocarcinomatous differentiation.
Nodular fasciitis (NF) is a benign proliferation of fibroblasts and myofibroblasts occurring most commonly in the upper extremities that can mimic a variety of mesenchymal tumors including sarcoma. Although reported in almost all anatomic locations, only 7 cases of intraneural nodular fasciitis have been reported in English literature. The gene fusion has not been previously reported in intraneural nodular fasciitis, although it has been reported in three entities including aneurysmal bone cyst, nodular fasciitis, and intravascular fasciitis.
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