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1.
J Craniofac Surg ; 23(2): 573-7, 2012 Mar.
Article in English | MEDLINE | ID: mdl-22446418

ABSTRACT

INTRODUCTION: The role of genetic phenomena has been given central importance in the development of craniosynostosis. Proponents have dismissed the role of force as a key etiologic factor. Nonetheless, compressive forces on the developing calvarium have been shown to result in premature suture fusion. The purpose of this study was to determine whether cyclical loading of the murine calvarium could induce suture fusion in cocultured calvarial specimens. MATERIALS AND METHODS: Calvarial coupons from postnatal day 21, B6CBA wild-type mice (n = 24) were harvested and cultured. A custom appliance capable of delivering compressive loads was applied perpendicular to the sagittal suture in vitro. Six coupons were subjected to 0.3 g of force for 30 minutes each day for a total of 14 days. Six additional coupons were cocultured within the same medium. Control groups were devised. Histologic analysis of suture phenotype was performed. RESULTS: Sagittal sutures cocultured with unloaded specimens remained patent. In contradistinction, 4 of 6 specimens cocultured with loaded coupons demonstrated craniosynostosis (P = 0.03). Increased osteoid, alkaline phosphatase staining, and bone sialoprotein expression were observed when compared with matched controls. DISCUSSION: An in vitro model of force-induced craniosynostosis via paracrine effects has been devised. Premature fusion of the murine sagittal suture was induced in unloaded specimens cocultured with cyclically loaded calvarial coupons. These results implicate that abnormal forces may act through soluble factors to cause premature suture fusion in vitro. The findings support our global hypothesis that epigenetic phenomena play a crucial role in the pathogenesis of nonsyndromic craniosynostosis.


Subject(s)
Cranial Sutures/growth & development , Craniosynostoses/genetics , Craniosynostoses/pathology , Paracrine Communication/genetics , Skull/growth & development , Alkaline Phosphatase/metabolism , Animals , Biomarkers/metabolism , Coculture Techniques , Cranial Sutures/metabolism , Cranial Sutures/pathology , Disease Models, Animal , Integrin-Binding Sialoprotein/metabolism , Mice , Phenotype , Skull/metabolism , Skull/pathology , Stress, Mechanical
3.
Plast Reconstr Surg ; 124(6): 1840-1848, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19952640

ABSTRACT

BACKGROUND: The cause of nonsyndromic craniosynostosis remains elusive. Although compressive forces have been implicated in premature suture fusion, conclusive evidence of force-induced craniosynostosis is lacking. The purpose of this study was to determine whether cyclical loading of the murine calvaria could induce suture fusion. METHODS: Calvarial coupons from postnatal day-21, B6CBA, wild-type mice (n = 18) were harvested and cultured. A custom appliance capable of delivering controlled, cyclical, compressive loads was applied perpendicular to the sagittal suture within the coupon in vitro. Nine coupons were subjected to 0.3 g of force for 30 minutes each day for a total of 14 days. A control group of nine coupons was clamped in the appliance without loading. Analysis of suture phenotype was performed using alkaline phosphatase and hematoxylin and eosin staining techniques and in situ hybridization analysis using bone sialoprotein. RESULTS: Control group sagittal sutures-which normally remain patent in mice-showed their customary histologic appearance. In contradistinction, sagittal sutures subjected to cyclic loading showed histologic evidence of premature fusion (craniosynostosis). In addition, alkaline phosphatase activity and bone sialoprotein expression were observed to be increased in the experimental group when compared with matched controls. CONCLUSIONS: An in vitro model of force-induced craniosynostosis has been devised. Premature fusion of the murine sagittal suture was induced with the application of controlled, cyclical, compressive loads. These results implicate abnormal forces in the development of nonsyndromic craniosynostosis, which supports our global hypothesis that epigenetic phenomena play a crucial role in the pathogenesis of craniosynostosis.


Subject(s)
Alkaline Phosphatase/metabolism , Cranial Sutures/growth & development , Craniosynostoses/pathology , Animals , Animals, Newborn , Biomarkers/analysis , Cranial Sutures/metabolism , Craniosynostoses/metabolism , Disease Models, Animal , Mice , Mice, Inbred CBA , Pressure , Probability , Random Allocation , Reference Values , Skull/growth & development , Skull/metabolism , Stress, Mechanical , Tissue and Organ Harvesting
4.
J Neurosurg Pediatr ; 4(6): 523-7, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19951037

ABSTRACT

Adams-Oliver syndrome is a rare congenital disorder that includes congenital scalp and skull defects, variable degrees of terminal transverse limb anomalies, and cardiac malformations. Cutis aplasia occurring in 75% of patients is a potentially life-threatening condition. Large skin defects that cannot be closed primarily present a management dilemma, and may require skin grafting or flaps, or a combination of both operative and conservative modalities. The authors' experience in management of huge scalp and bone defects with the Integra Dermal Regeneration Template and regular dressing changes showed good scalp repair and no serious complications attributed to this approach.


Subject(s)
Abnormalities, Multiple/therapy , Bandages , Dura Mater/injuries , Dura Mater/surgery , Ectodermal Dysplasia/complications , Neurosurgical Procedures , Scalp/abnormalities , Skin, Artificial , Skull/abnormalities , Ectodermal Dysplasia/therapy , Female , Hand Deformities, Congenital/complications , Humans , Hydrocephalus/complications , Hydrocephalus/diagnostic imaging , Imaging, Three-Dimensional , Infant, Newborn , Rupture, Spontaneous/complications , Skull/diagnostic imaging , Syndrome , Tomography, X-Ray Computed
5.
J Oral Maxillofac Surg ; 67(8): 1581-8, 2009 Aug.
Article in English | MEDLINE | ID: mdl-19615567

ABSTRACT

PURPOSE: The authors review their experiences during multiple cleft surgical missions to rural Bangladesh from 2006 to 2008. A significant number of patients who underwent primary palatoplasty or cheiloplasty were of adult age or size. Adult primary cleft lip and palate repair is often more challenging than repair at the standard age of fewer than 2 years. This patient population is rarely seen in the United States, but may be treated more often by American surgeons during surgical missions to the developing world. This report discusses the experiences of the authors' treatment of cleft lips and palates in rural Bangladesh. PATIENTS AND METHODS: One hundred forty-six cleft-lip and cleft-palate patients were treated during 3 missions to rural Bangladesh, from 2006 to 2008. Thirty-three (23%) patients were of adult size, and aged 13 to 35 years. One hundred thirteen (77%) patients were aged 12 years or younger. Unilateral cleft lips were repaired with a Millard advancement-rotation technique. Bilateral cleft lips were repaired via the 1-stage procedure advocated by Mulliken and Salyer. Cleft palates were repaired using a 2-finger flap method. RESULTS: Overall, 8 of 146 patients (5.5%) had nonlife-threatening complications (infection or wound dehiscence) requiring subsequent revision surgery. The adult-sized patients had clefts of significantly increased size secondary to patient growth, as well as maxillary expansion transversely and anteriorly. Adult cleft-lip repair required significant soft-tissue dissection to close the cleft adequately, and ensure symmetry to the upper lip and alar bases. However, this procedure sometimes resulted in placement of the lip cicatrix in an anatomically disadvantageous position. In addition, with the increased transverse dimension of the adult cleft palate, tension-free 3-layer closure was difficult. Again, aggressive dissection of the soft tissue was required: the nasal and muscular layers were closed without much tension, but oral closure was often under tension, requiring the assistance of dermal biomaterials to bolster the repair. CONCLUSIONS: Patients in the developing world often have limited access to specialized health care, and may not realize that cleft lips and palates can be repaired. As a result, there is an increased incidence of unrepaired clefts in adult-sized individuals in this part of the globe. The American surgeon may encounter these patients during surgical missions. The surgeon should be prepared to repair adult patients with clefts that are significantly enlarged in all 3 dimensions. Closure will require significant soft-tissue dissection as well as the use of biomaterials as needed to repair wide cleft palates.


Subject(s)
Cleft Lip/surgery , Cleft Palate/surgery , Medical Missions , Rural Health , Adolescent , Adult , Anesthesia, General , Bangladesh , Biocompatible Materials/therapeutic use , Child , Child, Preschool , Developing Countries , Dissection/methods , Follow-Up Studies , Humans , Infant , Intubation, Intratracheal , Medical Missions/organization & administration , Medical Missions/standards , Plastic Surgery Procedures/methods , Reoperation , Surgical Flaps , Surgical Wound Dehiscence/etiology , Surgical Wound Infection/etiology , Suture Techniques , Young Adult
6.
J Craniofac Surg ; 19(4): 913-22, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18650712

ABSTRACT

Burn trauma continues to injure an estimated 1 million children each year in the United States alone, with many more injuries suffered worldwide. Several decades ago, advances in acute burn wound management, including development of topical antimicrobials, dramatically improved outcomes in pediatric burn injuries. However, infection remains the leading cause of burn wound mortality. With increasing antibiotic resistance in many medical centers, precise selection of topical antimicrobial therapy has grown in importance for pediatric burn management. Effective choice and application of topical antimicrobials require correct classification of burn wounds, appropriate understanding of the process of burn wound sepsis, and accurate identification of pathogens for individual patients as well as for their surrounding environment. This article examines the current and evolving role of topical antimicrobials in pediatric burn wound management. Burn wound classification, the biologic process of burn wound sepsis, wound cultures with pathogen profiling, and evaluations of commonly used topical antimicrobials are reviewed. Newer biologically active occlusive (bio-occlusive) and hybrid products are examined in the context of topical antimicrobial therapy and their increasing role in pediatric burn wound management.


Subject(s)
Anti-Infective Agents/administration & dosage , Bacterial Infections/prevention & control , Burns/therapy , Occlusive Dressings , Wound Infection/prevention & control , Administration, Topical , Adolescent , Anti-Infective Agents/classification , Bacterial Infections/classification , Bacterial Infections/complications , Burns/classification , Burns/complications , Child , Child, Preschool , Humans , Infant , Wound Infection/classification , Wound Infection/complications , Wound Infection/microbiology
7.
Plast Reconstr Surg ; 117(7): 2243-9, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16772924

ABSTRACT

BACKGROUND: The goal in this study was to investigate the role of extracellular signal-related kinase (ERK) 1/2, a central regulator of mesenchymal stem cell differentiation, and its temporal relationship to bone morphogenetic protein (BMP) 2/4, a potent osteogenic growth factor, during live model distraction osteogenesis. METHODS: The authors examined histomorphometric expression through the early temporal sequence for both ERK 1/2 and BMP 2/4 during gradual distraction to 5.1 mm (n = 12 net). Comparison groups (group sizes, n = 12) included an acute critical-size defect of 5.1 mm and a subcritical-size defect of 2.1 mm. RESULTS: In the group gradually distracted to 5.1 mm, immunohistochemical analysis demonstrated significant intranuclear expression of ERK 1/2 within mesenchymal precursor cells at the osteotomy edges early in distraction (postoperative days 6 and 9). ERK 1/2 became increasingly localized to hypertrophic chondrocytes within the distraction regenerate during the later stages of distraction (postoperative day 16). Adjacent sections examined for BMP 2/4 expression established a close temporal and spatial correlation with ERK 1/2. BMP 2/4 expression was initially present in the regions surrounding mesenchymal precursor cells expressing ERK 1/2, but then developed most prominently within the cytoplasm of hypertrophic chondrocytes expressing ERK 1/2 late in distraction. Comparison groups consistently demonstrated either fibrous nonunion or bony union typical in fracture healing, depending on defect size. However, even specimens with subcritical-size defects and complete bony union were consistently found to have minimal ERK 1/2 expression. CONCLUSIONS: These data provide evidence that ERK 1/2 expression is present within mesenchymal precursor cells during distraction osteogenesis and that ERK expression correlates closely with BMP 2/4 expression. The presence of ERK 1/2 expression only during gradual distraction strongly implicates the concept that mechanical strain appears to be the key upregulating factor for ERK 1/2 expression, based on comparison with fracture-healing and critical-size defect specimens.


Subject(s)
Bone Morphogenetic Proteins/biosynthesis , Extracellular Signal-Regulated MAP Kinases/biosynthesis , Mandible/metabolism , Mechanotransduction, Cellular/physiology , Osteogenesis, Distraction , Animals , Cell Differentiation , Chondrocytes/metabolism , Fracture Healing/physiology , Male , Mandible/physiology , Mandible/surgery , Mesenchymal Stem Cells/physiology , Mitogen-Activated Protein Kinase 1/biosynthesis , Mitogen-Activated Protein Kinase 3/biosynthesis , Models, Animal , Osteogenesis/physiology , Osteotomy , Rats , Rats, Sprague-Dawley
8.
Ann Plast Surg ; 55(2): 207-15, 2005 Aug.
Article in English | MEDLINE | ID: mdl-16034255

ABSTRACT

Craniofacial distraction osteogenesis (DO) is an evolving reconstructive technique with expanding applications for the treatment of bony deficiencies of the facial skeleton. Mechanical force has been known to play a fundamental role in modulating sustained osteogenic response and therefore is believed to function as a critical regulator of DO. We hypothesize that key clustering components of an integrin-mediated signaling pathway, including c-Src (pp60), are necessary for mediating the response to mechanical force. The specific aim of this study is to demonstrate up-regulation of a key focal adhesion molecule, c-Src, selectively in new bone formation subject to the mechanical forces of distraction and to demonstrate a lack of that same up-regulation in new bone formation associated with simple fracture healing. An additional specific aim is to demonstrate colocalization of c-Src expression and bone morphogenetic protein (BMP 2/4) expression during mandibular DO. Using a rat model of mandibular DO, c-Src and BMP 2/4 expression were evaluated in critical size defects, subcritical size defects, and mandibles undergoing gradual distraction. Osseous regeneration was observed in the course of gradual distraction; this process was associated with increased expression of c-Src. Furthermore, the presence of BMP 2/4 closely approximated c-Src expression spatially and temporally, suggesting a link between cytoplasmic focal adhesion activation and the resultant nuclear regulation of osteogenic protein expression. In significant contradistinction, minimal c-Src expression was found in the subcritical-sized defects where the fractures healed secondarily but where no gradual distraction was performed. Instead, the new bone formation inherent in the secondarily healed subcritical-sized defects demonstrated expected BMP 2/4 expression but was devoid of an up-regulation of c-Src. Finally, as expected, minimal expression of both c-Src and BMP was found in fibrous nonunion specimens. C-src expression was observed during gradual distraction; furthermore, minimal c-Src expression was visualized during subacute and critical-size defect fracture healing. C-Src expression also closely approximated BMP expression during DO. These findings that c-Src expression is found primarily only during conditions of cyclic distraction forces strongly implicates that mechanical force during gradual distraction is associated with c-Src expression. These results provide in vivo support for previous in vitro evidence that mechanical force profoundly influences osseous regeneration during distraction osteogenesis by means of a c-Src dependent mechanotransduction pathway, resulting in increased expression of osteogenic proteins, including BMP 2/4.


Subject(s)
Bone Morphogenetic Proteins/genetics , Bone Regeneration/physiology , Integrins/physiology , Mandible/physiology , Mechanotransduction, Cellular/physiology , Neural Pathways/pathology , Osteogenesis, Distraction , Proto-Oncogene Proteins pp60(c-src)/genetics , Transforming Growth Factor beta/genetics , Animals , Bone Morphogenetic Protein 2 , Bone Morphogenetic Protein 4 , Focal Adhesion Kinase 1/genetics , Hypertrophy/pathology , Immunohistochemistry , Mandible/pathology , Protein-Tyrosine Kinases/genetics , Rats , Rats, Sprague-Dawley
9.
Pediatr Emerg Care ; 20(1): 40-2, 2004 Jan.
Article in English | MEDLINE | ID: mdl-14716166

ABSTRACT

Large lip avulsion injuries that involve significant tissue loss to the lip vermilion and other local landmarks can often pose a surgical dilemma for the reconstructive surgeon. Immediate reconstruction of these injuries are frequently performed using local flaps and adjacent tissue transfer to close the defect, but these repairs frequently suffer from the unfortunate consequence of increased associated scarring and further permanent distortion of the local anatomy. We present 2 patients sustaining dog bite injuries associated with extensive traumatic tissue loss to the lip vermilion and other local landmarks. These patients were treated conservatively with excellent functional and cosmetic results. A single minor surgical revision of 1 patient's cupid's bow was performed 1 year after injury. In cases of significant traumatic avulsion involving the lip vermilion and the perioral composite soft tissue, even with injuries including delicate anatomic landmarks, healing by secondary intention can be instituted as the initial treatment of choice in younger patients, often providing optimal results.


Subject(s)
Bites and Stings/therapy , Dogs , Facial Injuries/therapy , Lip/injuries , Wound Healing , Administration, Topical , Adult , Animals , Anti-Bacterial Agents/therapeutic use , Child , Cicatrix/prevention & control , Combined Modality Therapy , Esthetics , Facial Injuries/surgery , Female , Humans , Lip/surgery , Male , Plastic Surgery Procedures , Sunscreening Agents/therapeutic use , Suture Techniques , Treatment Outcome
10.
J Craniofac Surg ; 14(5): 803-8, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14501353

ABSTRACT

Pediatric mandibular distraction osteogenesis (MDO) has become a mainstay of treatment for patients with micrognathia and retrognathia. As craniofacial surgeons have gained experience with MDO, the technique has become a safe and durable means of mandibular lengthening that avoids the significant morbidity of conventional surgical treatments. The full impact of this technique has not yet been realized for pediatric patients. Although studies have confirmed durable reconstruction of mandibular length with MDO, the range of applications of this technique is currently limited. As innovative clinicians continue to apply MDO to pediatric clinical craniofacial problems not easily treated with conventional means, the field of MDO will continue to mature. This article discusses current uses and examples of potential future applications of pediatric MDO. The development of novel and creative applications of MDO will advance the management of complex craniofacial anomalies, taking the field of craniofacial surgery into the future.


Subject(s)
Mandibular Advancement/methods , Osteogenesis, Distraction , Retrognathia/surgery , Sleep Apnea, Obstructive/surgery , Child, Preschool , Cleft Palate/complications , Female , Humans , Infant , Male , Mandible/abnormalities , Mandible/surgery , Pierre Robin Syndrome/complications , Retrognathia/etiology , Sleep Apnea, Obstructive/etiology
11.
Ann Plast Surg ; 49(5): 511-9, 2002 Nov.
Article in English | MEDLINE | ID: mdl-12439020

ABSTRACT

Despite the increasing use of distraction osteogenesis (DO) of the mandible, the molecular mechanisms regulating new bone formation during DO remain poorly understood. The purposes of this study were (1) to establish a unique rodent model of DO capable of outlining parameters for new bone formation at the distraction site and (2) to determine a critical-size defect to differentiate osteogenesis resulting from distraction from conventional fracture healing at the osteotomy site. Adult Sprague-Dawley rats were fitted successfully with this newly developed distraction device. Analyses demonstrated that the device could distract the rat mandible reliably to 5.1 mm with complete union. Acute intersegmental gaps of 2 mm resulted in complete bony union in a manner consistent with fracture healing, whereas 3-mm acute gaps resulted in varying degrees of bony union. Acute intersegmental gaps of 5.1 mm invariably resulted in fibrous nonunion. In summary, the authors have developed a rodent model of DO of the mandible. Their distraction protocols resulted successfully in advancement to 5.1 mm with bony consolidation. Notable fracture healing occurred at immediate intersegmental spaces as large as 3 mm. A gap of 5.1 mm was sufficient to act as a critical-size defect, resulting consistently in fibrous nonunion. These findings validate the effectiveness of this distraction device and establish the critical-size defect of a rat mandible at more than 3 mm. This novel model of DO provides an effective method of examining fundamental mechanisms responsible for new bone formation in the craniofacial skeleton.


Subject(s)
Mandible/surgery , Models, Animal , Osteogenesis, Distraction/methods , Animals , Fracture Healing , Mandibular Fractures/physiopathology , Mandibular Fractures/surgery , Osteogenesis/physiology , Osteotomy , Rats , Rats, Sprague-Dawley
12.
J Craniofac Surg ; 13(4): 497-500, 2002 Jul.
Article in English | MEDLINE | ID: mdl-12140410

ABSTRACT

Cutis aplasia (or aplasia cutis congenita) is a congenital absence of all skin layers, often extending through bone. This defect usually occurs in the scalp and can be extensive, exposing the dura mater, and deeper meninges. Treatment regimens for cutis aplasia have included early operative intervention, including skin and bone grafts, local scalp flaps, or free flaps to close the defect. In addition to the significant perioperative risks, these invasive procedures may inhibit the osteogenic potential of the dura to initiate and sustain bony closure of the defect. We report a case of an infant with Adams-Oliver syndrome and cutis aplasia involving a large portion of the skull that was treated conservatively with topical Silvadene dressings. No surgical treatment of bone or soft tissue reconstruction was necessary. This case report is the first to our knowledge to document complete bony restoration of the cranial vault through serial three-dimensional CT scans. The intensive therapeutic intervention in this case report allowed early discharge from the hospital, a gradual amelioration of the patient's alopecia as the hair-bearing scalp slowly covered the defect, and precluded the need for any subsequent bony reconstruction of the cranial vault. We hypothesize that conservative treatment of cutis aplasia maintains dural induction of osseous regeneration, and any treatment plan for bony defects of cutis aplasia should consider maintenance of dural integrity. Although further investigation is warranted, an initial trial of antimicrobial dressing care might optimally promote secondary closure of the cranial vault without the need for surgical intervention.


Subject(s)
Anti-Infective Agents, Local/therapeutic use , Bone Regeneration/physiology , Ectodermal Dysplasia/drug therapy , Parietal Bone/abnormalities , Scalp/abnormalities , Silver Sulfadiazine/therapeutic use , Administration, Cutaneous , Administration, Oral , Alopecia/therapy , Anti-Infective Agents/administration & dosage , Anti-Infective Agents/therapeutic use , Anti-Infective Agents, Local/administration & dosage , Bandages , Dura Mater/physiopathology , Ectodermal Dysplasia/physiopathology , Female , Follow-Up Studies , Humans , Infant, Newborn , Longitudinal Studies , Osteogenesis/physiology , Parietal Bone/growth & development , Scalp/growth & development , Silver Sulfadiazine/administration & dosage , Tomography, X-Ray Computed , Trimethoprim, Sulfamethoxazole Drug Combination/administration & dosage , Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic use
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