Giant cell carcinoma of the lung (GCCL) is a rare histological form of large-cell lung carcinoma a subtype of undifferentiated lung cancer traditionally classified within the non-small cell lung carcinomas […]
List of articles in "Disease" category - Page 40
Embryonal rhabdomyosarcoma
Embryonal rhabdomyosarcoma (ERMS) is a rare histological form of cancer of connective tissue wherein the mesenchymally-derived malignant cells resemble the primitive developing skeletal muscle of the embryo. It is the […]
Radial scar
In breast pathology a radial scar of the breast formally radial scar of the breast and also known as complex sclerosing lesion of the breast or simply complex sclerosing lesion […]
Complement 3 deficiency
Complement 3 deficiency is a genetic condition affecting complement component 3.It can cause systemic lupus erythematosus-like symptoms.It can lead to an increase in pyogenic infections from encapsulated bacteria.
Bednar’s aphthae
Bednar’s aphthae is a type of oral ulceration (mouth ulcers) which occurs in infants. The lesions are located on the palate and are caused by trauma. No treatment is required […]
Pancreatic abscess
Pancreatic abscess is a late complication of acute necrotizing pancreatitis occurring more than 4 weeks after the initial attack. A pancreatic abscess is a collection of pus resulting from tissue […]
Endosalpingiosis
In gynecology endosalpingiosis is a condition in which fallopian tube-like epithelium is found outside of the fallopian tube. It is unknown what causes this very rare condition and it may […]
Sarcomatoid carcinoma
Sarcomatoid carcinoma is a relatively uncommon form of cancer whose malignant cells have histological cytological or molecular properties of both epithelial tumors (carcinoma) and mesenchymal tumors (sarcoma).
Fraley syndrome
Fraley syndrome is a condition where the superior infundibulum of the upper calyx of the kidney is obstructed by the crossing renal (upper or middle section) artery branch causing distension […]
Paris-Trousseau syndrome
Paris-Trousseau syndrome (PTS) is an inherited disorder characterized by mild hemorrhagic tendency associated with 11q chromosome deletion.FLI1 has been suggested as a candidate.