A rare case report of solitary neurofibroma arising in the male breast. [PDF]
Parkhurst EL, Chan SM.
europepmc +1 more source
MRI features of nipple leiomyoma in a male patient: A case report. [PDF]
Ando S +6 more
europepmc +1 more source
A Rare Case of Adenoid Cystic Carcinoma in the Male Breast: Clinical Presentation and Histopathological Evaluation. [PDF]
Tayebi N, Jahanbin B, Nozheh A.
europepmc +1 more source
A case report: Diagnosis and treatment of idiopathic hypertrophic pachymeningitis
We reported a case of idiopathic hypertrophic dura meningitis diagnosed in our hospital. The patient repeatedly suffered from headaches, followed by blurred vision in the right eye. During this period, multiple sclerosis was considered for diagnosis, and it improved after hormone treatment.
Zhong Luo +7 more
wiley +1 more source
A rare presentation of male breast atypical papillary lesion. [PDF]
Soltani K +4 more
europepmc +1 more source
Abstract Lynch syndrome (LS) is the most common hereditary colorectal cancer syndrome, caused by a germline pathogenic variant in one of the mismatch repair (MMR) genes. Among these, MSH6‐associated LS represents a distinct subtype with unique molecular and clinical characteristics.
Salwa Ben Yahia +4 more
wiley +1 more source
Association Between Red Blood Cell Distribution Width-To-Albumin Ratio and Breast, Colorectal, Lung, and Prostate Cancers. [PDF]
Habibzadeh P, Sorkin J, Hsu D.
europepmc +1 more source
Cardiovascular disease incidence and cancer risk in two large European prospective cohorts
What's New? Cardiovascular disease (CVD) and cancer share risk factors and biological mechanisms, raising questions about potential associations between the two, particularly regarding CVD duration and cancer onset. Whether CVD influences subsequent cancer risk, however, remains inconclusive.
Emma Fontvieille +25 more
wiley +1 more source
Risk of Malignancy with Immunosuppressive Drugs Used in Organ Transplants Compared to Those Used for Non-Transplant Indications. [PDF]
Haines C +6 more
europepmc +1 more source

