Results 1 to 10 of about 1,118 (255)

Surgical rarities: case report of appendicular diverticulitis and literature review. [PDF]

J Surg Case Rep, 2022
Abstract Appendicular diverticulosis is a rare condition observed in about 0.004–2% of all appendectomy specimens. Risk of perforation/bleeding is high and a relevant association with mucinous neoplasms is known. Appendectomy is indicated even in case of occasional finding.
Bonomo LD, Zago M, Quirico C, Ottinetti A, Panzera F, Galli A, Gattoni L, Canova G, Nicotera A.   +8 more
europepmc   +5 more sources

Italian Bird Rarities Committee (COI) - Report 29

Avocetta, 2021
Italian Birds Rarities Committee (COI) - Report 29. This report refers to records from January 1st to December 31st 2019, with the addition of a number of records from previous years that were submitted more recently.
Egidio Fulco, Cristiano Liuzzi
doaj   +4 more sources

Intramuscular desmoplastic fibroblastoma: a case report of extreme rarities in extremities. [PDF]

J Surg Case Rep, 2021
AbstractSoft tissue tumors are part of a wide and sometimes rare differential diagnostic landscape. Case description of these rare soft tissue masses helps the future differentiation and aids in preoperative multidisciplinary approach. Interpretation and staging, with the help of imaging, is key.
Onghena L, Verniers L, Woussen S, Van den Broecke C, Fierens K, Van Kerschaver O.   +5 more
europepmc   +5 more sources

Polyostotic Fibrous Dysplasia: A Case Report of Rarity [PDF]

Cureus, 2023
A skeletal condition known as fibrous dysplasia (FD) is characterized by the replacement of healthy bone with fibrous bone tissue. One bone (monostotic) or several bones could be involved (polyostotic). Any bone in the body might become affected by FD. The skull and face bones are the most typical locations.
Sanjana N Wadewale, Nitin Bhola, Anchal Agarwal   +2 more
openalex   +3 more sources

Li-Fraumeni Syndrome, A Rarity Among Rarities: A Case Report and Review of Literature. [PDF]

Cureus, 2023
Li-Fraumeni syndrome (LFS) is a rare inherited cancer susceptibility disorder with a wide tumour spectrum, particularly in children and young adults. Patients with LFS have life-long cancer risk, and the most commonly encountered tumours include soft tissue sarcoma, breast cancer, brain tumours, osteosarcoma, leukaemia and adrenocortical carcinoma. LFS
Elremeli M, Idaewor P, Rasheed N, Saad Abdalla Al-Zawi A.   +3 more
europepmc   +3 more sources

Oral squamous papilloma: report of a clinical rarity [PDF]

BMJ Case Reports, 2013
Oral squamous papilloma is a benign proliferation of the stratified squamous epithelium, which results in a papillary or verrucous exophytic mass induced by human papilloma virus (HPV).1 ,2 A 51-year-old, healthy steel plant male worker reported with complaint of growth on lower lip near the left corner of mouth since 2 years.
Anand Pratap Singh, Supreet Jain, TR Chaitra, Adwait Kulkarni   +3 more
openalex   +3 more sources

Diversifying participation: The rarity of reporting racial demographics in neuroimaging research

NeuroImage, 2022
Functional neuroimaging has been instrumental to the field of cognitive neuroscience; however, its increasing prevalence has evoked conversations concerning limitations associated with reproducibility and bias. Prevailing racial, cultural, and socioeconomic biases in scientific research perpetuate demographic homogeneity in participation, contributing ...
Madeline G. Goldfarb, Darin R. Brown
openalex   +4 more sources

Exudative Benign Cementoblastoma with Radiographic Rarities- A Case Report with Review of Literature [PDF]

Journal of Clinical and Diagnostic Research, 2022
Cementoblastoma is a rare benign odontogenic neoplasm of mesenchymal origin. The benign cementoblastoma was previously classified as one of the cementoma neoplasias by the World Health Organisation’s (WHO) classification of odontogenic tumours.
CJ Sanjay, Karthikeya Patil, D Saikrishna, Nagabhushana Doggalli, A Shiny   +4 more
doaj   +2 more sources

Colonic Goblet Cell Carcinoid: Rarity of a Rarity! A Case Report and Review of Literature

Chirurgia, 2020
Goblet cell carcinoids (GCC) are extremelyrare neuroendocrine tumours, and characterised by their unique combination of two types of cancer cells âÃÂ" neuroendocrine (carcinoid) and epithelial (adeno-carcinoma). In spite of the fact that GCC is regarded as Neuro-Endocrine Tumour (NET), it does not illicit carcinoid syndrome. GCC usually arises in the
Abdalla Saad Abdalla Al‐Zawi, Kashuf A Khan, Ahmed Shah, Amira Asaad, Victoria Salter, Marina Barron, Soad Eldruki, Victoria Salih, Salem Alowami   +8 more
openalex   +3 more sources

Unveiling a Rarity: A Case Report on Glomangiopericytoma in the nasal cavity [PDF]

Indian Journal of Otolaryngology and Head & Neck Surgery, 2023
Sino-nasal glomangiopericytoma is a rare benign tumour comprising only about 0.5% of all sino-nasal tumours. Presenting as a bleeding nasal mass, it is among the myriad of differential diagnoses for the same. Clinical characterisation of mass becomes difficult; hence, histopathology and immunohistocytochemistry play an essential role in clenching the ...
Akshat Kushwaha, Ngohlaki Khaimeichho, Sreerekha Jinkala, Lokesh Kumar Penubarthi   +3 more
openalex   +3 more sources