Autophagic vacuolar cardiomyopathy is an underrecognized, but potentially fatal, complication of treatment with chloroquine (CQ) and its derivative hydroxychloroquine (HCQ), which are used as therapy for malaria and common connective tissue disorders.
Currently, the diagnosis of autophagic vacuolar cardiomyopathy is established through an endomyocardial biopsy and requires electron microscopy, which is not widely available and has a significant potential for sampling error. (...)
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Most recent articles
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drug-induced autophagic vacuolar cardiomyopathy
22 May -
NUP62
22 Mayinfo DKFZp547L134, FLJ20822, FLJ43869, IBSN, MGC841, "nuclear pore glycoprotein p62", p62, SNDI; info nucleoporin 62kDa WP
Diagnostic use
autophagic vacuolar cardiomyopathy Autophagic vacuolar cardiomyopathy is an underrecognized, but potentially fatal, complication of treatment with chloroquine (CQ) and its derivative hydroxychloroquine (HCQ), which are used as therapy for malaria and common connective tissue disorders. Currently, the diagnosis of autophagic vacuolar (...) -
cytoplasmic positivity of TTF-1
22 Maycytoplasmic positivity of TTF1 eIHC
Cytoplasmic staining with TTF-1 has been little studied. This cytoplasmic staining is due to a cross-reacting antigen of 160 kd, which is not an alternative splicing product of TTF-115.
In a large series of consecutive cases, about 6% (23/361) of all tumours from a variety of sites showed cytoplasmic staining.
hepatocellular carcinoma
a minority of pulmonary adenocarcinomas show coarse granular cytoplasmic staining
occasionally in squamous (...) -
CA-125
22 MayWP 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. -
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 (...)
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