Neuropsychiatric manifestations occur in a minority of systemic lupus erythematosus (SLE) patients and can present with a diverse spectrum of symptoms, complicating the diagnosis and treatment. This report discusses a case involving a 58-year-old female patient who experienced an...
Open access
Research Article10.9734/ajcrmh/2025/v8i1236
KIKUCHI-FUJIMOTO disease (KFD), or HISTIOCYTIC NECROTIZING LYMPHADENITIS, is a benign and self-limited disease that mainly affects young women. Patients present with localized lymphadenopathy, fever, and leukopenia in up to half of the cases. It was first described by Dr Masahiro...
Open access
Research Article10.9734/ajcrmh/2025/v8i1235
Behçet’s disease (BD) is a rare systemic vasculitis with an unclear etiology, infrequently associated with hematologic malignancies. We report a 27-year-old man with severe mucocutaneous BD who developed acute myeloblastic leukemia (AML-1) following a SARS-CoV-2 infection. The pa...
Open access
Research Article10.9734/ajcrmh/2025/v8i1234
This case report discusses a rare presentation of transient neonatal pustular melanosis (TNPM) in a full-term newborn. The female infant, born via vaginal delivery at [38 weeks], presented shortly after birth with characteristic pustular lesions that rapidly evolved into hyperpig...
Open access
Research Article10.9734/ajcrmh/2025/v8i1233
Birdshot's chorioretinopathy is a well-known form of posterior uveitis, often chronic, bilateral and of unknown etiology. Its prevalence varies between 0.69 and 1.73 cases per 100,000 population. It is characterized by multiple, distinctive, hypopigmented choroidal lesions, and i...
Open access
Research Article10.9734/ajcrmh/2025/v8i1232
In the context of cancer prevalence in India, breast cancer is the most common leading site for women, followed by cervical cancer.1 Globally, kidney cancer accounts for approximately 2% of all neoplasms and cases of extramammary malignancies metastasizing to the breast are extre...
Open access
Research Article10.9734/ajcrmh/2025/v8i1231
Werner syndrome (WS), or adult progeria, is a rare autosomal recessive disorder characterized by premature aging and multisystem involvement. Its initial presentation through a metabolic emergency remains exceptional. We report the case of a 41-year-old woman with a history of ch...
Open access
Research Article10.9734/ajcrmh/2025/v8i1230
Aim: This case report emphasises the hope for distressed patients with follicular lymphoma, highlighting the impact of rituximab-based immunochemotherapy on the prognosis and quality of life of a patient treated at Redeemers Health Village, a multi-specialty tertiary academic hos...
Open access
Research Article10.9734/ajcrmh/2025/v8i1229
We report a rare association of Late Onset Combined Immunodeficiency (LOCID) with epidermodysplasia verruciformis (EV) in a 23-year-old Moroccan woman. At age 7, the patient developed thousands of small verrucae and experienced recurrent respiratory and gastrointestinal infection...
Open access
Research Article10.9734/ajcrmh/2025/v8i1228
Budd-chiari syndrome is a condition in which hepatic venous outflow is obstructed. Budd-Chiari Syndrome is a rare but serious condition that can lead to significant liver damage if not diagnosed and treated early. Budd-Chiari syndrome (BCS) has a low incidence and prevalence; res...
Open access
Research Article10.9734/ajcrmh/2025/v8i1226