Arterial anatomy of the hallucal sesamoids.

The aim of this study was to analyze the arterial supply of the sesamoid bones of the hallux. Twenty-two feet from adult cadavers were injected with epoxide resin or an acrylic polymer in methyl methacrylate (Acrifix) and subsequently processed by two slice plastination methods and the enzyme maceration technique. Afterwards, the arterial supply of the sesamoid bones was studied. The first plantar metatarsal artery provided a medial branch to the medial sesamoid bone. The main branch of the first plantar metatarsal artery continued its course distally along the lateral side of the lateral sesamoid and supplied it. The supplying arteries penetrated the sesamoid bones on the proximal, plantar, and distal sides. The analysis and cataloging of the microvascular anatomy of the sesamoids revealed the first plantar metatarsal artery as the main arterial source to the medial and lateral sesamoid bones. In addition, the first plantar metatarsal artery ran along the lateral plantar side of the lateral sesamoid bone, suggesting that this artery is at increased risk during soft-tissue procedures such as hallux valgus surgery.

The microvascular anatomy of the metatarsal bones: a plastination study.

PURPOSE: The purpose of this study was to categorize and systematize the arterial supply of the metatarsal bones and furthermore the observation of arterial lesions after frequently performed forefoot surgeries. MATERIALS AND METHODS: Twenty-two cadaver feet were analyzed by two plastination methods and the enzyme maceration method. Five forefoot surgeries were performed after arterial injections. RESULTS: The bases of the metatarsal bones were primarily supplied by dorsal and plantar arteries. The arterial supply of the metatarsal diaphysis was given by a frequently observed nutrient artery. The first plantar metatarsal artery was the main supply of the first metatarsal head. The plantar and dorsal metatarsal arteries supplied the lesser metatarsals heads. The forefoot surgeries revealed lesions of arteries in all cases. CONCLUSIONS: The plastination methods were excellent methods to analyze the arterial supply. In addition arterial damage after forefoot surgeries could be analyzed with these methods.

Functional gliding spaces of the dorsal side of the human hand.

The clinical and functional importance of gliding spaces of the hand (e.g., their role in the spread of infection or as a consideration in reconstructive surgery) has been repeatedly emphasized. However, only a few studies have provided details regarding the connective tissue spaces in the metacarpal region of the dorsal side of the human hand. The aim of the present study was to analyze the morphology and elucidate the anatomic relation of functional gliding spaces in the metacarpal region on the dorsal side of the human hand in order to provide a better understanding of function, and of clinical disorders and their treatment. To delineate these spaces we used a plastic (Acrifix 90) injection method. Twenty fixed and unfixed cadaver hands were subcutaneously injected with Acrifix 90 (a methacrylate) into the metacarpophalangeal transitional region and into the tendon sheaths of the extensor muscles. Different colors were used to distinguish one injected plastic solution from another. The spreading pattern of the injected medium was analyzed by careful dissection. To delineate the exact bordering structures and the topography of the injected spaces, two hands were plastinated using the E12/E6 technique (von Hagens et al., Anat Embryol 1987;175:411-421), and one hand was injected and embedded in Technovit 7100 for histological investigations. Injecting the plastic into the metacarpophalangeal transitional region of fingers II-IV in a disto-proximal direction, the solution spreads along the surface of the separate extensor tendons. It then coalesces 1-2 cm proximal to the injection points to form a continuous plastic plate, which protrudes between and on top of the previous injected tendon sheaths. In no case was a communication between the paratendinous tissue and the tendon sheaths observed. Laterally, the injected solution is delimited at the radial side of the extensor tendon of the second finger and at the ulnar side of the extensor tendon of the fourth finger. Using the described technique at the fifth finger yields a plastic plate that extends from the injection point to the tendon sheath. However, in two specimens a connection between the plastic injected into the tendon sheath of the fifth finger, and the distal injected solution was observed.