Maxillary Artery Traversing Through the Temporal Muscle.

Few previous dissection reports demonstrated the possible course of the maxillary artery (MA) through the temporalis muscle (TM). A dissection study performed a long time ago established a 2% prevalence of this variant. As the variant was not studied on angiograms, we decided to do so. One hundred seventy archived computed tomography angiograms were used on 95 male and 75 female patients. The MA course through the TM was found in 11/170 cases (6.47%) but in 16/340 sides (5.58%). This is because, in 5/11 cases, the variant was bilateral. Therefore, preoperative computed tomography angiography could be helpful when surgical procedures using either the TM or the MA are designed. The course of the MA is variable, either deep or through the TM.

Fenestrated Maxillary Artery.

The external carotid artery divides terminally into the superficial temporal and maxillary arteries (MA), deep to the base of the neck of the mandible. Arterial fenestrations are commonly found in the vertebrobasilar and internal carotid systems but are rarely encountered, or reported, in the external carotid artery system. The archived computed tomography angiograms of a 70-year-old male patient were observed anatomically. Inferior to the posterior end of the lateral pterygoid muscle was found a fenestrated segment of the MA, oriented mediolaterally. The middle meningeal artery left the superior arm of that fenestration. The inferior arm of the fenestration gave off a temporoalveolar trunk, further divided into posterior deep temporal and inferior alveolar arteries. The MA fenestration and the temporoalveolar trunk are rare variations of the MA at the entrance in the infratemporal fossa. These make the MA prone to iatrogenic lesions during different surgical procedures addressed to this region.

Lymphatic lacunae of the human eye conjunctiva embedded within a stroma containing CD34+ telocytes.

An accurate identification of telocytes (TCs) was limited because of the heterogeneity of cell types expressing the markers attributed to TCs. Some endothelial lineage cells also could fit within the pattern of TCs. Such endothelial cells could line conjunctival lacunae previously assessed by laser confocal microscopy. We have been suggested that an accurate distinction of TCs from endothelial cells in the human eye conjunctiva could be achieved by use of CD31, CD34 and D2-40 (podoplanin); and that the conjunctival lacunae are in fact lymphatic. We aimed as testing the hypothesis by an immunohistochemical study on human eye conjunctiva biopsy samples. Samples of human eye conjunctiva from 30 patients were evaluated immunohistochemically by use of the primary antibodies: CD34, D2-40 and CD31. D2-40 was equally expressed within epithelia and laminae propria. Basal epithelial cells were D2-40 positive. Within the stromal compartment, the lymphatic marker D2-40 labelled several lymphatic vessels. CD31 labelled both vascular and lymphatic endothelial cells within the lamina propria. When capillary lymphatics were tangentially cut, they gave the false appearance of telocytes. Blood endothelial cells expressed CD34, whereas lymphatic endothelial cells did not. Stromal CD34-expressing cells/telocytes were found building a consistent pan-stromal network which was equally CD31-negative and D2-40-negative. The conjunctival lymphatic lacunae seem to represent a peculiar anatomic feature of eye conjunctiva. They are embedded within a CD34-expressing stromal network of TCs. The negative expression of CD31 and D2-40 should be tested when discriminating CD34-expressing TCs.

Endocardial tip cells in the human embryo - facts and hypotheses.

Experimental studies regarding coronary embryogenesis suggest that the endocardium is a source of endothelial cells for the myocardial networks. As this was not previously documented in human embryos, we aimed to study whether or not endothelial tip cells could be correlated with endocardial-dependent mechanisms of sprouting angiogenesis. Six human embryos (43-56 days) were obtained and processed in accordance with ethical regulations; immunohistochemistry was performed for CD105 (endoglin), CD31, CD34, α-smooth muscle actin, desmin and vimentin antibodies. Primitive main vessels were found deriving from both the sinus venosus and aorta, and were sought to be the primordia of the venous and arterial ends of cardiac microcirculation. Subepicardial vessels were found branching into the outer ventricular myocardium, with a pattern of recruiting α-SMA+/desmin+ vascular smooth muscle cells and pericytes. Endothelial sprouts were guided by CD31+/CD34+/CD105+/vimentin+ endothelial tip cells. Within the inner myocardium, we found endothelial networks rooted from endocardium, guided by filopodia-projecting CD31+/CD34+/CD105+/ vimentin+ endocardial tip cells. The myocardial microcirculatory bed in the atria was mostly originated from endocardium, as well. Nevertheless, endocardial tip cells were also found in cardiac cushions, but they were not related to cushion endothelial networks. A general anatomical pattern of cardiac microvascular embryogenesis was thus hypothesized; the arterial and venous ends being linked, respectively, to the aorta and sinus venosus. Further elongation of the vessels may be related to the epicardium and subepicardial stroma and the intramyocardial network, depending on either endothelial and endocardial filopodia-guided tip cells in ventricles, or mostly on endocardium, in atria.