Karl Schwaiger

Split-thickness skin grafting for reconstruction of auricular skin defects: a statistical analysis

Surgical reconstruction following the removal of large malignant auricular lesions is challenging. While many options for defect closure have been described, in the elderly population usually affected flap surgery, long anesthesia times, patient compliance, and anticoagulant therapy pose additional risks. An alternative quick, simple, and effective method of defect closure is therefore highly desirable. The objective of the present study was to assess the aesthetic outcome, healing process, complications, and recurrence rates associated with unmeshed split‐thickness skin grafts (STSGs) used for covering large auricular skin defects following cartilage‐sparing skin cancer removal.

Trigger Finger Caused by Extraskeletal Chondroma

Chondroma is a relatively rare, but well-reported benign neoplasm. This lesion normally occurs attached to bone; however, they may be rarely found without association to bone and embedded in soft tissue. The authors describe the case of a 76-year-old man in whom flexor tendon triggering was associated with an extraskeletal chondroma between the annular ligament and the flexor tendon.

Spalthauttransplantation zur Defektdeckung am Ohr: eine statistische Analyse

Die Rekonstruktion nach Entfernung ausgedehnter maligner Hauttumoren am Ohr ist eine Herausforderung. Verschiedene Methoden der Defektdeckung wurden beschrieben. Lappenplastiken, längere Anästhesiezeiten, geringe Compliance und Antikoagulation stellen bei den oft älteren Patienten zusätzliche Risiken dar. Eine rasch, effizient und unkompliziert durchführbare Methode der Defektdeckung ist daher wünschenswert. Ziel der Studie war die Beurteilung des ästhetischen Resultats, des Heilungsprozesses, der Komplikations‐ und Rezidivrate nach Transplantation ungenetzter Spalthaut (SPHT) zur Defektdeckung nach knorpelerhaltender Resektion maligner Tumoren am Ohr.

Hailey–Hailey Disease and Reduction Mammoplasty: Surgical Treatment of a Gene Mutation

Level of Evidence V This journal requires that authorsassign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of

Localized hypertrichosis after index finger revascularization and complex regional pain syndrome.

Various skin changes have been described in complex regional pain syndrome (CRPS), but the association of hypertrichosis with finger replantation has not been described in literature. CRPS occurs as the inadequate response to painful trauma in a distal extremity. Clinically, two types of CRPS can be differentiated according to the preceding noxious event without (CRPS I) or with (CRPS II) an obvious nerve lesion [1]. CRPS I (sympathetic reflex dystrophy) is characterized by sensory disturbances, burning deep spontaneous pain, and allodynia. Disturbances in the skin blood circulation, sweating, edema, and trophic disturbances of the skin, joints, and bones are typical and not limited to the region of the peripheral nerves. CRPS II (causalgia) appears following a partial peripheral nerve lesion, but the symptoms are identical [1]. Regarding the pathogenetic mechanism involved in CRPS, no consensus exists, but trauma-related cytokine release, neurogenic inflammation, sympathetically maintained pain, and cortical reorganization in response to chronic pain seem to play a key role in the development and maintenance of this complex pain syndrome [2]. We describe a patient who developed a mild form of CRPS with an evident localized hypertrichosis on the hand and forearm after subtotal amputation and revascularization of the distal phalanx of the index finger. A 26-year-old woman presented with a traumatic subtotal amputation of the distal phalanx of the right index finger caused by a woodworking machine. Under general anesthesia, two crossed Kirschner wires were used for bony fixation, and for revascularization, the proper digital artery supplying the ulnar side and two dorsal veins were repaired. Both digital nerves were intact. The immediate postoperative course was uneventful, but on the third postoperative day, a thrombosis of the reconstructed artery occurred, which required surgical revision. Under general anesthesia and continuous brachial plexus blockade, reconstruction and revascularization were performed by interposition of a vein graft from the forearm. Continuous brachial plexus blockade for increased blood flow to the injured extremity and postoperative pain management were retained for 5 days. Postoperatively, the index finger was dressed with gauze and a simple hand bandage. Occupational therapy was started 2 weeks postoperatively. About 5 weeks after surgery, the patient presented with a swelling and a glassy dermal texture of the index finger and the hand with expansion to the forearm. Active range of motion was reduced, but the patient did not complain about severe pain. Occupational therapy was continued and calcitonin, in the form of a nasal spray, was prescribed. Six weeks later, a distinct local hypertrichosis of the right hand and forearm was observed, even though at this time, edema and functional impairment had nearly disappeared (Fig. 1). Six months after surgery, the patient was free of complaints, and the localized hypertrichosis was in involution. Fig. 1 (A) Right hand with local hypertrichosis. (B) Left hand. CRPS is a complex syndrome that is most often initiated by trauma to an extremity, such as fractures, surgical wounds, and crush injuries. It is rarely attributed to other injuries such as venipuncture, burns, electrical injuries, inflammatory processes, and spinal cord injuries. Unusual precipitating events supposedly account for CRPS, including central nervous system lesions, peripheral vascular bypass procedures, and carpal tunnel syndrome. The exact pathomechanism of this complex syndrome is not clarified, but the major mechanisms, which might occur subsequently or in parallel during the course of CRPS, are trauma-related cytokine release, dysfunction of thermoregulation, neurogenic inflammation, sympathetically maintained pain, and cortical changes in response to pain [2]. Further, molecular biological examination has pointed to an association with human leukocyte antigen (HLA), and the opinion that CRPS has a psychosomatic background is also popular [2]. Although in our case, the chronic pain was not ostensible, four of the five symptoms (unexplained diffuse pain, altered skin color, altered skin temperature, edema, and reduced active range of motion) were present to justify the diagnosis of CRPS. Unilateral functional inhibition of sympathetic vasoconstrictor neurons seems to be a characteristic feature of acute CRPS and is unlikely to be responsible for the skin warming and vasodilatation. Therefore, continuous brachial plexus blockade for increased blood flow to the injured extremity and postoperative pain management could have been a trigger in the development of CRPS in our patient. Regarding the therapy of this complex syndrome, efficient pain therapy (non-steroidal anti-inflammatory drugs and opioids) and pharmacologic medical treatment (sympatholytics, anticonvulsants, corticoids, antidepressants, anxiety medications, and calcitonin), aside from occupational therapy, are mainly responsible for a good clinical outcome [1]. In case of deficient improvement of disorders, an invasive treatment (stellate ganglion and other nerve blocks) can be discussed. However, in our case, the conservative therapy concept with cooling and keeping the affected finger in an elevated position as often as possible, as well as the intensive occupational therapy (active and passive extension/flexion exercises of the whole hand), were sufficient to disrupt the vicious circle of CRPS and to obtain good hand function. Whether intranasal calcitonin application has a positive effect, is controversial in the literature [3]. Localized hypertrichosis has been reported to develop at the site of malignancies, psoralen+ultraviolet-A light therapy, and infection (chickenpox scars); at the periphery of burned skin; in the leg after radical inguinal lymphadenectomy; and after topical use of diverse medicaments (such as minoxidil, prostaglandine, and glucocorticoids) and is also reported in connection with CRPS [4]. Pathogenically, we postulate that the cutaneous hyperemia, as a part of the CRPS, induced the hypertrichosis by stimulating the hair follicles [5]. Further, the anxious personality of our patient, the fear of overloading the transplanted finger, and the subsequent prolonged immobilization, could have played a key role in the manifestation of the symptoms.