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IMCAS Academy

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VOLVER

IMCAS Asia 2025
Programa

Non-sponsored scientific lectures

Sala: Open Stage - Level 2
Fecha: domingo 8 junio 2025 de 09:00 a 11:30
Formato: CHARLA EN ESCENARIO ABIERTO > presentaciones orales grabadas en un escenario dedicado dentro del área de exposición

Las presentaciones

Horas	Oradores	Título de la presentación	Resumen	Número
09:00	Dr Monisha KAPOOR	Beyond hair transplant, non-invasive follicular auto stem cell implantation: The future is here!	Ver	148854
09:12	Dr Barry DEKEYSER	Personalized PRP and class 4 Er:YAG laser therapy for androgenetic alopecia: A case study with optimized trichoscopy-guided treatment protocols	Ver	148928
09:24	Dr Ayano OKUDA	Diversifying intimate area treatments: Changes and current status of pubic hair removal and female genital plastic surgery in our clinic	Ver	148937
09:36	Dr Shunsuke NAGURA	New developments in thread lifting in Japan: Effective techniques combining thread lifting and fat-suction injections	Ver	149477
09:48	Dr Mehmet CIMEN	Safety and efficacy analysis of plant-based exosome treatments for androgenetic alopecia	Ver	149126
10:00	Dr Lehavit AKERMAN	Porsthetic hair injection a novel treatment for androgenetic alopecia in female patients: A retrospective case series analysis	Ver	149473
10:12	Dr Kyung Tae BAE	Tailored filler strategies based on rheological properties: A scientific approach to facial aesthetics	Ver	149474
10:24	Dr Suparuj LUEANGARUN	Synergistic effects of Fractional Picosecond Laser (FPL) and Rose Stem Cell-Derived Exosomes (RSCEs) in acne scar treatment: A split-face pilot study	Ver	149475
10:36	Dr Ratchathorn PANCHAPRATEEP	A power of combination: Hair transplantation and autologous micrografting	Ver	149478
10:48	Dr Panji RESPATI	Effectiveness of autologous cellular micrograft kit in hair restoration for androgenetic alopecia: A novel case series	Ver	149479

Ver la sala anterior (LUNCH BREAK)

Ver la sala siguiente (LUNCH BREAK)

Sesiones recomendadas

Alopecia (pérdida de cabello)

Transplante capilar

Exosomas

Factores de crecimiento

Células madre

Dr Monisha KAPOOR

Cirujano Plástico

India

Otro(s) autor(es) :

Beyond hair transplant, non-invasive follicular auto stem cell implantation: The future is here!

Objectives: The objective of this study is to introduce a new cutting edge, non-surgical and non-invasive solution which provides a quick recovery for patients of various types of hair losses except infective scalp diseases. To eliminate the dependency on donor hair by reactivating the patient’s own dormant follicles, thereby enabling the potential for unlimited natural hair regrowth.

Introduction: Follicular Stem Cell Implantation (FSCI) is a revolutionary, non-surgical solution to hair loss that leverages the body’s natural regenerative capabilities. In contrast to conventional hair loss therapies or hair transplants. This personalized approach stimulates dormant follicles, promotes natural hair growth, and addresses issues like thinning and premature greying without the need for daily medication or donor hair.

Materials / method: The study was conducted in Dr. Monisha Kapoor aesthetics. It is an observational study done for a period of 10 months. This technique isolates and multiplies follicular stem cells in a certified laboratory for a month using a scalp biopsy and about 25 hair strands. These cells are then injected into the scalp after one month over three sessions a month apart. 15 patients have completed 3 sessions of the follicular stem cell implantation therapy and 5 patients that are undergoing the procedure currently.

Results: The patients showed a marked reduction in hair shedding, increased density, increased shaft thickness and overall satisfactory results. Built on years of scientific research, FSCI offers a permanent, minimally invasive alternative for restoring healthy, thick hair across all stages and various types of hair loss in all the genders.

Conclusion: This study highlights the effectiveness of Follicular Stem Cell Implantation (FSCI) as a ground-breaking, non-surgical solution for hair loss. The observed results demonstrate significant improvements in hair density, reduction in shedding, and high patient satisfaction, supporting FSCI as a safe, regenerative alternative to traditional treatments

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Tiene vínculos financieros con alguna entidad que podría llegar a competir estrechamente con los medicamentos, materiales o instrumentos tratados en su investigación?
No

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

Dr Barry DEKEYSER

Anestesiólogo

Bélgica

Otro(s) autor(es) :

Personalized PRP and class 4 Er:YAG laser therapy for androgenetic alopecia: A case study with optimized trichoscopy-guided treatment protocols

Objectives: This presentation provides a structured, trichoscopy-guided approach to diagnosing and treating androgenetic alopecia (AGA). A case study is presented in which platelet-rich plasma (PRP) therapy was progressively optimized over 18 months, combined with Class 4 Er:YAG laser therapy for enhanced follicular stimulation. The stepwise refinement of PRP concentration and volume will be detailed, offering a personalized strategy for hair loss management.

Introduction: Hair loss is a major concern for millions worldwide, yet effective non-surgical solutions remain challenging. Many patients discontinue treatment due to suboptimal results or lack of clear guidance. While PRP therapy is widely used, its efficacy is highly dependent on concentration, volume, and application protocols. This case study highlights how a systematic, personalized PRP protocol—combined with the latest Class 4 Er:YAG laser technology—can optimize patient outcomes.

Materials / method: A 44-year-old female patient with persistent AGA was treated with a progressively refined PRP protocol and Er:YAG laser therapy:
1. Trichoscopy-based diagnosis, including AI-assisted follicular density mapping.
2. PRP optimization over four phases in 18 months, adjusting concentration (target: 1,000,000 platelets/µL) and volume (5 mL plasma).
3. Class 4 Er:YAG laser therapy (2940 nm, long-pulse mode) applied at key treatment milestones for enhanced follicular activation and vascular stimulation.
Patient progress was monitored using standardized clinical photography.

Results: Results:
• Significant improvement in hair density confirmed by standardized clinical photography.
• Patient-reported hair quality improvement, leading to discontinuation of cosmetic camouflage (hairpiece use).
• No adverse effects or complications, confirming the safety and tolerability of the combined treatment approach.

Conclusion: This case study demonstrates the critical importance of optimizing PRP concentration and volume in achieving consistent and effective results in AGA treatment. The combination of personalized PRP protocols with Class 4 Er:YAG laser therapy presents a novel, non-invasive strategy for enhanced follicular regeneration. Further clinical studies are needed to establish standardized guidelines for this promising multimodal approach.

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Tiene vínculos financieros con alguna entidad que podría llegar a competir estrechamente con los medicamentos, materiales o instrumentos tratados en su investigación?
Si
Por favor especifique las entidades (individuo, empresa, sociedad): Arthrex (Trainer), Fotona (Clinical Lecturer)

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

Dr Ayano OKUDA

Dermatólogo

Japón

Otro(s) autor(es) : Hidetoshi Muramatsu

Diversifying intimate area treatments: Changes and current status of pubic hair removal and female genital plastic surgery in our clinic

Objectives: The objective of this study is to analyze trends in the number of procedures and patient demographics related to pubic hair removal and Female genital plastic surgery, in order to clarify changes in demand for these treatments. Additionally, the study aims to evaluate the impact of the widespread adoption of pubic hair removal on Female genital plastic surgery and to identify trends in labia minora reduction choices.

Introduction: Intimate area treatments are gaining global attention, and in Japan, procedures such as pubic hair removal are becoming increasingly diverse and widespread. In this report, we present the history and current status of pubic hair removal and female genital plastic surgery at our clinic.

Materials / method: We investigated the number of patients who underwent pubic hair removal and female genital plastic surgery at our clinic between 2007 and 2024. In addition, we conducted a questionnaire survey (from May to November 2024) targeting 187 first-time patients seeking labia minora reduction, the most common type of female genital plastic surgery. The survey included questions about age, chief complaints, presence or absence of pubic hair removal, and home care practices such as the use of special soaps or creams.

Results: Pubic hair removal patients increased from 751 in 2007 to 5,179 in 2024, 7 times increase. Female genital plastic surgery patients grew from 35 to 302, 8.6 times increase. In 2007, 5.7% of patients were in their teens to 30s, with 94.2% in their 40s to 70s. By 2024, 66.7% were in their teens to 30s, and 33.3% in their 40s to 70s. For labia minora reduction, ages ranged from 18 to 64, avg 32.2. Reasons for surgery: discomfort (51.3%), pigmentation (37.9%), and asymmetry (28.3%). 58.2% had pubic hair removal, and 22.2% said it led to interest in labiaplasty. 35.2% used home care.

Conclusion: We are seeing a clear increase in demand for pubic hair removal and female genital plastic surgery, especially among younger patients. With the influence of social media and the increasing availability of commercial products and services, public interest in intimate area treatments appears to be expanding. Understanding patients’ backgrounds and motivations is crucial as these procedures continue to gain popularity and evolve as medical practices.

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Tiene vínculos financieros con alguna entidad que podría llegar a competir estrechamente con los medicamentos, materiales o instrumentos tratados en su investigación?
No

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

Dr Shunsuke NAGURA

Cirujano Plástico

Japón

Otro(s) autor(es) :

New developments in thread lifting in Japan: Effective techniques combining thread lifting and fat-suction injections

Objectives: Facial aging typically involves both volume loss and expansion, leading to sagging and a bloated lower face. While thread lifting is commonly used to address this, its effects are often short-lived. To enhance and prolong results, the combination of thread lifting and a novel “fat-suction injection” technique is gaining popularity. This study aims to evaluate the clinical efficacy of this approach, known as the Suction Lift, in treating facial sagging.

Introduction: Between 2020 and 2023, the demand for aesthetic procedures in Japan tripled, particularly for minimally invasive treatments with minimal downtime. Facial contouring is now the second most popular procedure after blepharoplasty, and among these, the combination of thread lifting with liposuction—known as the “Suction Lift”—has gained significant attention. We developed a new liposuction technique called the “fat-suction injection,” which uses fine cannulas to minimize downtime. This method has since been widely adopted by many aesthetic surgeons in Japan.

Materials / method: Ten cases of Suction Lift procedures performed between June and August 2024 were analyzed. Preoperative and six-month postoperative facial contours and volume changes were compared using 3D Vectra imaging. Overlay analysis was conducted to evaluate the precise differences in volume and contour.

Results: Compared to thread lifting alone, combining thread lifting with liposuction improved lifting effects and resulted in more sustained contour changes over time.

Conclusion: The addition of liposuction to thread lifting enhances the tissue contraction and re-adhesion effects typically achieved with thread lifts. Moreover, the volume reduction from liposuction—which may otherwise increase the risk of sagging—can be compensated by the lifting effect of threads, creating a synergistic outcome. This approach may be especially effective for patients with moderate to severe sagging who seek stronger and longer-lasting results. Additionally, we will present 3D imaging analysis of volume changes following thread lift alone.

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Tiene vínculos financieros con alguna entidad que podría llegar a competir estrechamente con los medicamentos, materiales o instrumentos tratados en su investigación?
No

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

Dr Mehmet CIMEN

Médico

Turquía

Otro(s) autor(es) :

Safety and efficacy analysis of plant-based exosome treatments for androgenetic alopecia

Objectives: This study aims to share the results of 1,500 exosome treatments administered to hair transplant and non-transplant individuals over one year. Exosomes play a crucial role in cell-to-cell components in regenerative medicine. Their application in scalp treatments has demonstrated promising results. This presentation highlights the importance of exosomes in improving treatment outcomes for androgenetic alopecia with overall patient satisfaction

Introduction: Plant-derived exosomes are emerging as a safe and effective cell-free therapy for scalp regeneration. In this study, we selected the HRLV exosome formulation due to its RSCE (Root Stem Cell Extract) content, which is rich in miRNA-122-5p. This specific miRNA has been shown to counteract the effects of DHT on hair follicles by reducing inflammation and promoting follicular cell survival, making HRLV a promising option for androgenetic alopecia management.

Materials / method: A total of 1,500 exosome treatments were conducted from September 2023 to March 2025 with Exocobio HRLV (RSCE) product in Doku Clinic. The study assessed the efficacy and short-term safety of these treatments, focusing on both patients who
underwent hair transplantation and those who did not. Clinical outcomes were monitored through regular follow-ups and evaluations of hair growth, scalp health, and patient satisfaction with 3 month 6 months 1 year before after pictures.

Results: Results from this extensive study will be discussed in detail, emphasizing the differences in treatment outcomes between individuals who received hair transplants and those who did not. Key metrics will include the rates of hair growth, scalp health improvement, and any reported adverse effects. Visual aids, including images, will be used to illustrate the results, and a thorough analysis of the proportionate outcomes will be elaborated upon during the presentation.

Conclusion: The findings from this study will provide valuable insights into the safety and effectiveness of plant-based rose stem cell exosome treatments for androgenetic alopecia. This research has the potential to enhance current treatment protocols and improve patient outcomes in the field of hair restoration.

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

Dr Lehavit AKERMAN

Dermatólogo

Israel

Otro(s) autor(es) :

Porsthetic hair injection a novel treatment for androgenetic alopecia in female patients: A retrospective case series analysis

Objectives: A retrospective analysis of the efficacy and safety of new generation of prosthetic hair implants as a treatment for androgenetic alopecia in 25 woman.

Introduction: Androgenetic alopecia is one of the most common conditions and is a stressful experience for both sexes, but substantially more distressing for women. Women with androgenetic alopecia possess a more negative body image and a pattern of less adaptive functioning. Although this is a verry common condition we still lack a non surgical effective treatment and surgical restoration remains the only reliable method to restore hair in women with sever alopecia. Therefore there is a need for an additional non-surgical treatment option to to restore hair.

Materials / method: 25 patients (ages 41-68) underwent prosthetic hair injection between 2020-2024. Patients underwent a test procedure in which 48 hairs were implanted to make sure there is no adverse reaction and 6-10 weeks later patients underwent full treatment (768-1152 hairs). Patients underwent between 1-3 treatment sessions with prosthetic hair fibers (by Hairstetics LTD)which are made of two biocompatible materials: nitinol and nylon and are preloaded on sterile disposable cartridges 12 hair fibers on each. Side effects and patient satisfaction rate were monotored 6-18 months post procedure.

Results: All patients that were chosen to undergo this treatment had good clinical improvement and over 80% mentioned that it improved their self confidence and body image. Side effects were mostly mild and included focal erythema and papular lesions (in 5 patients overall). No patients needed an extraction of the implants.

Conclusion: The new generation of prosthetic hair implants is a safe and effective procedure mainly for woman with stable and severe androgenetic alopecia- since there is a need for a reliable minimally invasive procedure .It can serve as an additional tool for patients which are looking for an office procedure rather a surgical one. Patient selection is crucial for positive outcome. More studies are needed to establish the long term outcome.

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Tiene vínculos financieros con alguna entidad que podría llegar a competir estrechamente con los medicamentos, materiales o instrumentos tratados en su investigación?
No

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

Dr Kyung Tae BAE

Médico

Corea del Sur

Otro(s) autor(es) :

Tailored filler strategies based on rheological properties: A scientific approach to facial aesthetics

Objectives: This study aims to establish a clinically applicable strategy for selecting hyaluronic acid (HA) fillers based on rheological properties—specifically, gel firmness (G’), flexibility (xStrain), and cohesivity. The goal is to enhance safety, predictability, and aesthetic outcomes by tailoring filler selection and injection techniques according to facial anatomy and movement dynamics.

Introduction: Facial aging is a multilayered process involving volume loss, ligament laxity, and changes in skin elasticity. HA fillers have become essential in aesthetic medicine, but product selection often lacks scientific grounding. Understanding rheological behavior provides an objective framework to select appropriate fillers for specific anatomical needs—balancing support, mobility, and natural integration.

Materials / method: We analyzed the rheological characteristics (G’, xStrain, cohesivity) of commonly used HA fillers using data from published literature and in vitro measurements. A region-specific treatment algorithm was developed using a layer-by-layer anatomical model. Clinical case reviews and visual assessments were conducted to evaluate volume retention, mobility adaptation, and patient satisfaction post-treatment.

Results: High G’ fillers demonstrated superior lifting capacity and volume retention in structurally deficient areas such as the midface and chin. High xStrain fillers provided natural animation and improved integration in dynamic zones like lips and nasolabial folds. The layer-specific approach minimized complications such as lumpiness, migration, and unnatural appearance, enhancing overall treatment satisfaction.

Conclusion: Filler rheology plays a critical role in achieving safe and natural aesthetic results. Scientific understanding of viscoelastic properties and their clinical implications enables practitioners to deliver customized, anatomy-driven treatments. A rheology-based filler strategy supports both function and form—leading to reproducible outcomes and higher patient satisfaction in facial rejuvenation.

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Tiene vínculos financieros con alguna entidad que podría llegar a competir estrechamente con los medicamentos, materiales o instrumentos tratados en su investigación?
No

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

Dr Suparuj LUEANGARUN

Médico Internista

Tailandia

Otro(s) autor(es) : Suparuj Lueangarun , Byong Seung Cho, Therdpong Tempark

Synergistic effects of Fractional Picosecond Laser (FPL) and Rose Stem Cell-Derived Exosomes (RSCEs) in acne scar treatment: A split-face pilot study

Objectives: To evaluate the clinical efficacy and safety of combining RSCEs with FPL in reducing atrophic acne scars by assessing post-treatment recovery, scar severity reduction, and adverse effects.

Introduction: Fractional Picosecond Laser (FPL) has been shown to be effective in treating atrophic acne scars. However, there is a need for improved post-treatment recovery and enhanced overall efficacy. Stem cell-derived exosomes have demonstrated potential as a cell-free therapy for tissue regeneration and recovery. Recently, interest has grown in plant-based exosomes, such as Rose Stem Cell-Derived Exosomes (RSCEs), which offer similar regenerative benefits. This study investigates the synergistic effects of FPL and RSCEs in treating atrophic acne scars.

Materials / method: A prospective, double-blind, randomized split-face pilot study on atrophic acne scars involved a single FPL session with dual fluences, RSCE application on one side, and a control gel on the other. Patients used a topical exosome moisturizer for 21 days, with assessments at 1 and 3 months post-treatment, including photography, IGA ratings, biometric analyses, and recovery monitoring.

Results: The RSCE-treated side showed significantly greater reductions in acne scar severity scores compared to the control side. RSCE-treated areas exhibited milder erythema, shorter recovery times, and reduced post-treatment pain. No severe adverse effects were observed. At follow-up visits, the RSCE-treated sides displayed improved skin texture, enhanced scar appearance, and fewer residual scars compared to the control.

Conclusion: The combination of FPL and RSCEs is a safe and effective approach for treating atrophic acne scars, promoting faster recovery and superior scar improvement compared to standard treatments. As a plant-based exosome therapy, RSCEs hold great potential for broader applications in aesthetic and regenerative dermatology.

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Tiene vínculos financieros con alguna entidad que podría llegar a competir estrechamente con los medicamentos, materiales o instrumentos tratados en su investigación?
No

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

Dr Ratchathorn PANCHAPRATEEP

Dermatólogo

Tailandia

Otro(s) autor(es) :

A power of combination: Hair transplantation and autologous micrografting

Objectives: Bring more clinical evidence to support autologous micrografting technique (AMT) in the use with hair transplant (HT) surgery to enhance graft survival, improve wound healing in donor area and stop the progression of androgenetic alopecia in the non-transplanted area.

Introduction: One of the primary limitations of hair transplantation is the extended recovery period, frequently accompanied by post-procedural telogen effluvium. Surgical stress can disrupt the normal hair cycle of non-transplanted follicles, prematurely shortening the anagen phase and resulting in transient shedding. The healing of both donor and recipient sites may require up to two months, potentially impacting patient satisfaction and overall outcomes. Another concern is the variable survival rate of transplanted grafts, influenced by surgical technique, graft handling, and patient-specific factors.

Materials / method: We propose AMT, used in AGA, as an adjunctive treatment in HT surgery. This procedure involves mechanical disaggregation of skin biopsies from the occipital region, creating a cell suspension with regenerative biocomponents. Also, grafts obtained during FUE can be utilized to prepare the AMT suspension. It delivers cytokines for wound healing, ECM components supporting follicle integrity and cells with regenerative potential. When injected into recipient and donor areas immediately before the implantation phase can foster optimal conditions for graft survival and enhance postsurgical recovery

Results: The 1500 clinical cases and work over 10 years have shown that there is a reduction of the percentage of transplanted hair shedding after surgery. Additionally, the donor area heals much faster without scarring and necrosis preserving that area in case of future treatments. AMT shows good improvement over the non-transplanted miniaturized hairs.

Conclusion: In summary, AMT has demonstrated to accelerate tissue repair in donor area and to reduce post-transplant effluvium, improve graft survival in the recipient area and prevent AGA progression in the non-transplanted follicles. This method represents a promising biological approach to optimizing clinical outcomes in hair restoration surgery.

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Tiene vínculos financieros con alguna entidad que podría llegar a competir estrechamente con los medicamentos, materiales o instrumentos tratados en su investigación?
No

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

Dr Panji RESPATI

Dermatólogo

Indonesia

Otro(s) autor(es) : Reiva Farah Dwiyana

Effectiveness of autologous cellular micrograft kit in hair restoration for androgenetic alopecia: A novel case series

Objectives: To evaluate the clinical efficacy of autologous cellular micrograft (ACM) therapy in patients with androgenetic alopecia (AGA), focusing on improvements in hair thickness and density after treatment.

Introduction: AGA is a chronic condition affecting up to 80% of men, marked by follicle miniaturization. Traditional therapies often lack consistent results. ACM therapy, derived from HF-MSCs, offers a regenerative approach. This study explores ACM’s clinical use in AGA, aiming to provide evidence of its efficacy and safety.

Materials / method: Two male AGA patients (ages 36 and 38) received ACM therapy. Three 2-mm scalp biopsies were processed with microlyzer blades (600 μm and 150 μm) to create a cell suspension, which was injected into hormone-sensitive scalp areas. Hair thickness and density were evaluated at 2-month follow-up.

Results: Both patients showed visible increases in hair density and thickness after 2 months. No side effects were reported. Patient satisfaction was high, supporting ACM as a promising, minimally invasive treatment for both early and advanced stages of AGA.

Conclusion: ACM therapy offers a novel, well-tolerated solution for AGA by reactivating follicular stem and progenitor cells. Early results are encouraging, but larger studies are needed to confirm long-term benefits and broader clinical applicability.

Declaraciones

¿Ha recibido algún tipo de financiamiento para realizar su investigación sobre esta temática?
No

¿Ha recibido algún pago, honorario u otra compensación por su trabajo acerca de esta investigación?
No

¿Tiene vínculos financieros con alguna entidad que podría llegar a competir estrechamente con los medicamentos, materiales o instrumentos tratados en su investigación?
No

¿Posee o ha solicitado una patente relacionada a los materiales, productos o instrumentos utilizados en su investigación?
No

Este trabajo no cuenta con el apoyo de ningún financiamiento directo o indirecto. El autor asume plena responsabilidad sobre el mismo.

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