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List of articles in "Disease" category - Page 40

Giant-cell carcinoma of the lung

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 […]


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.


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