WP PO
CA-125 (cancer antigen 125 or carbohydrate antigen 125) also known as "mucin 16" or "MUC16" is a protein that in humans is encoded by the MUC16 gene.
MUC16 is a member of the mucin family glycoproteins.
CA-125 has found application as a tumor marker or biomarker that may be elevated in the blood of some patients with specific types of cancers, or other benign conditions.
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CA-125
22 May -
mediastinal lymph nodes
21 May -
Bowenoid papulosis
20 MayBowenoid papulosis consists of one or more indolent, verrucous papules on the genitalia with a clinical resemblance to condyloma acuminatum and a histological resemblance to Bowen’s disease.
HPV-16 is the most frequently detected HPV subtype detected in this condition. It usually responds to local therapies, but recurrences and the development of invasive carcinoma have been reported.
The term ‘penile intraepithelial neoplasia’ (PIN) has been coined to encompass the three preinvasive (...) -
penile intraepithelial neoplasia
20 MayThe term ‘penile intraepithelial neoplasia’ (PIN) has been coined to encompass the three preinvasive clinical entities of:
penile Bowen disease
erythroplasia of Queyrat
bowenoid papulosis. -
intraepidermal carcinoma
20 Mayintraepidermal carcinomas
Although the term ‘intraepidermal carcinoma’ is often used synonymously with Bowen disease, it is used here in a broader sense to include not only carcinoma in situ of the skin (Bowen’s disease), and penis (erythroplasia of Queyrat), but also intraepidermal epithelioma of Jadassohn, a controversial entity of disputed histogenesis.
Paget’s disease is sometimes included in this category because of the presence of cytologically malignant cells within the epidermis. (...) -
splenic amyloidosis
19 Mayspleen amyloidosis
PO
Synopsis
Macroscopy
firm consistency
waxy consistency
possible sago spleen
possible lardaceous spleen
splenomegaly
diffuse splenic infiltration
possible localized splenic nodules
rare splenic rupture
Microscopy
splenic deposition of pink amorphous material deposition of pink amorphous material limited either to germinal follicles (sago spleen) deposition of pink amorphous material along splenic sinusoids deposition of pink amorphous material in (...) -
splenic infectious mononucleosis
18 MayPO
Microscopy
expansion of red pulp immunoblastic proliferation in red pulp Immunoblasts may have strikingly atypical morphology, resemble Reed-Sternberg cells immunoblastic infiltration of subintima of intratrabecular veins Immunoblasts are positive for B and T cell markers, EBV by in situ hybridization, variable CD30
red pulp hemophagocytosis
Differential diagnosis
Hodgkin lymphoma
splenic localization of leukemia
splenic (...) -
spleen in hereditary spherocytosis
18 MayPO
Digital slides
UI:742 : spleen in hereditary spherocytosis.
Macroscopy
Microscopy
marked congestion of red pulp
empty appearance of sinuses (actually contain ghost red blood cells)
* may have prominent endothelial lined sinuses
red pulp hemosiderin deposition
red pulp erythrophagocytosis
Videos
Hereditary spherocytosis by Washington Deceit
See also
erythrocytic (...) -
spleen in hemolytic anemia
18 MayTypes of hemolytic anemia
congenital hemolytic anemia hereditary spherocytosis sickle cell anemia
acquired hemolytic anemia deposition of immune complexes on red blood cell membranes bacterial hemolysins plasma lipid abnormalities parasites
immune hemolytic anemia brucellosis Hodgkin lymphoma leukemia sarcoidosis SLE (lupus) tuberculosis
Microscopy
splenic congestion in cords and sinuses
splenic hemosiderin deposition
splenicextramedullary hematopoiesis (...) -
spleen in AIDS
18 May, by AdminPrior to highly active antiretroviral therapy (HAART), typical findings were:
white pulp depletion
red pulp hemosiderin deposition
splenic spindle cell proliferation
splenic perivascular hyalinization
also infectious and malignant infiltrates (Mod Pathol 2002;15:406)
Post-highly active antiretroviral therapy (HAART) findings include less frequent white pulp depletion, but similar rates of splenic involvement by atypical mycobacteria and CMV in those with systemic (...)
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