1.Treatment of allergic rhinitis in children by attenuating oxidative stress from sweat pore-Qi-triple energizer system.
China Journal of Chinese Materia Medica 2025;50(5):1419-1426
Sweat pores function is the ascending and descending of Qi. The human body maintains a continuous, holistic, and dynamic balance through the functioning of sweat pores as well as the Qi movement and transformation in the spleen, stomach, and triple energizer. Sweat pores play a crucial role in the generation and development of Zang-fu organs, essence and spirit, and body and orifices, as well as in the onset and progression of diseases. Oxidative stress significantly affects the regulation of inflammation in allergic rhinitis(AR), induces the pathological damage to nasal epithelial cells, and alters immune activity, serving as a key mechanism exacerbating AR symptoms. This mechanism closely aligns with the pathogenesis associated with dysfunction in the sweat pore-Qi-triple energizer system. In recent years, oxidative stress and antioxidants in AR have received increasing attention. Elevated levels of reactive oxygen species, fractional exhaled nitric oxide, and malondialdehyde have become key indicators for the early diagnosis of AR. Classical prescriptions, empirical prescriptions, and newly developed preparations of traditional Chinese medicine(TCM) for external use with anti-inflammatory, anti-allergic, and immune-regulatory effects via antioxidant pathways have demonstrated definite efficacy in treating AR. This provides a basis for understanding the pathogenesis of AR in TCM from a modern medical perspective. Therefore, this paper systematically examines the relationship between the sweat pore-Qi-triple energizer system and AR, incorporating the oxidative stress mechanism into the research on pathogenesis of the disorders. Furthermore, methods for treating AR in children are proposed with TCM preparations for external use which aimed at opening nasal sweat pores, dispersing, searching, channeling with aroma, warming, and dredging, regulating Qi movement in spleen, warming Yang Qi to promote urination, and clearing latent wind to inhibit liver depression.
Humans
;
Oxidative Stress/drug effects*
;
Rhinitis, Allergic/metabolism*
;
Child
;
Qi
;
Sweat/metabolism*
;
Drugs, Chinese Herbal/administration & dosage*
;
Medicine, Chinese Traditional
2.Research advances on the regulatory mechanism of sweat secretion ion channels of eccrine sweat glands.
Chinese Journal of Burns 2022;38(8):794-798
Sweat glands are widely distributed in human skin, among which eccrine sweat glands play major roles in heat dissipation and sweat secretion. Sweat secretion is mainly regulated by nervous system and includes two processes of secretion of secretory coil and reabsorption of sweat duct, involving various ion channels and proteins such as calcium ion channel, potassium ion channel, sodium-potassium-chloride co-transporter 1, Best2 protein, aquaporin 5, cystic fibrosis transmembrane conductance regulator, and epithelial sodium ion channel. This paper reviews the nerve conduction system and various ion channels involved in sweat secretion of exocrine sweat glands in order to provide a theoretical basis for the study of regeneration, repair, and transformation of stem cells.
Eccrine Glands/metabolism*
;
Humans
;
Sweat/metabolism*
3.Research advances on signaling pathways affecting sweat gland development and their involvement in the reconstitution of sweat adenoid cells in vitro.
Dong Hao LANG ; Te BA ; Sheng Jun CAO ; Fang LI ; Hang DONG ; Jun Liang LI ; Ling Feng WANG
Chinese Journal of Burns 2022;38(2):195-200
The damage of sweat glands in patients with extensive deep burns results in the loss of thermoregulation, which seriously affects the quality of life of patients. At present, there are many researches on the repair of sweat gland function, but the mechanism of human sweat gland development has not been fully clarified. More and more studies have shown that the cascaded pathways of Wnt/β-catenin, ecto- dysplasin A/ectodysplasin A receptor/nuclear factor-κB, sonic hedgehog, and forkhead box transcription factor jointly affect the development of sweat glands, and it has been reported that the cascaded signaling pathways can be used to achieve the reconstruction of sweat adenoid cells in vitro. This article reviews the signaling pathways that affect the development of sweat glands and their involvement in the reconstruction of sweat adenoid cells in vitro.
Adenoids/metabolism*
;
Hedgehog Proteins/metabolism*
;
Humans
;
Quality of Life
;
Signal Transduction
;
Sweat/metabolism*
;
Sweat Glands/physiology*
4.Research advances on the application of stem cells in sweat gland regeneration.
Jing Juan ZHANG ; Mao Ying WANG ; Jie ZHAO ; Du Yin JIANG
Chinese Journal of Burns 2022;38(3):296-300
Sweat gland is one of the important appendage organs of the skin, which plays an important role in thermoregulation and homeostasis maintenance. Sweat glands are damaged and unable to self-repair after burns, resulting in perspiration disorders eventually. However, current clinical strategies cannot restore the function of the damaged sweat glands effectively. Therefore, it is urgent to seek treatments that can promote the regeneration of sweat glands and restore their normal functions. Stem cells have extensive sources, low immunogenicity, high proliferation capacity, and multi-directional differentiation potential, which have become a focus in the field of regenerative medicine. In recent years, a variety of stem cells have been induced to differentiate into sweat gland-like tissue with certain secretory function, which provides treatment direction for sweat gland regeneration after burns in clinic. This article reviews the recent research advances on the application of stem cells in sweat gland regeneration from the perspectives of the manner by which stem cells transform into sweat gland cells in different environments and their influencing factors.
Cell Differentiation/physiology*
;
Regeneration/physiology*
;
Skin
;
Stem Cells
;
Sweat Glands/physiology*
5.Syringocystadenoma Papilliferum arising from a nevus sebaceus mimicking squamous cell carcinoma in a Filipino female: A case report
Maria Kristina R. Fajardo ; Daisy King-Ismael ; Bernardita O. Policarpio
Journal of the Philippine Dermatological Society 2021;30(1):37-40
Introduction:
Syringocystadenoma papilliferum (SCAP) is a relatively rare benign adnexal skin tumor which can manifest in a
variety of clinical forms. Nearly one-third of cases are known to develop within a pre-existing nevus sebaceus (NS). The peculiar
feature of this case was the appearance of a large exophytic tumor within a congenital verrucous plaque, which raised the
suspicion of a malignant transformation. This is a case of a young Filipino adult with an unusual presentation of syringocystad-
enoma papilliferum in a nevus sebaceus mimicking squamous cell carcinoma.
Case report:
A 27-year-old Filipino female presented a persistently enlarging exophytic pedunculated cribriform tumor within
a congenital verrucous plaque on the left temporal area. The tumor started to appear when she was 20 years old. One month
prior to consult, it rapidly increased in size and bled on gentle manipulation. She has neither comorbidities nor any family history
of a similar condition. Her physical examination was normal, with no palpable lymphadenopathies. The biopsy showed syringo-
cystadenoma papilliferum on a nevus sebaceus. She underwent carbon dioxide (CO2
) laser excision under local anesthesia. The
procedure was uneventful and the patient is on regular follow-up and close monitoring for any possible malignant change or
recurrence.
Conclusion
A case of syringocystadenoma papilliferum on a nevus sebaceus mimicking squamous cell carcinoma in a Filipino
female treated with carbon dioxide laser excision was presented. The unusual presentation of SCAP can mimic malignancy and
histopathologic evaluation is warranted to rule out malignant transformation for proper management.
Tubular Sweat Gland Adenomas
6.Selection of surgical strategies for vulvar Paget's disease.
Yu LIU ; Zheng-Yong LI ; Ai ZHONG ; Wijaya Wilson ADRIAN ; Jing PENG ; Jun-Jie CHEN
Chinese Medical Journal 2021;134(20):2483-2485
7.Dental Management in a Patient with Congenital Insensitivity to Pain with Anhidrosis : A Case Report
Cheolhyeon BAE ; Daewoo LEE ; Jaegon KIM ; Yeonmi YANG
Journal of Korean Academy of Pediatric Dentistry 2019;46(4):416-421
Congenital insensitivity to pain with anhidrosis (CIPA) is a rare, autosomal recessive disorder; affected patients are characterized by inability to feel pain and to sweat over the entire body, as well as by mental retardation. Because, in the oral examination, no specific findings on soft or hard tissue may be found except possible lesions due to self-mutilation, early recognition and diagnosis are essential for these patients. Pediatric dentists must be aware of the clinical manifestations and treatment considerations related to uncontrolled body temperature, tactile hyperesthesia and lack of pain reflex. In this case report, dental management of CIPA was suggested by presenting a 6-year follow-up of young patient.
Body Temperature
;
Dentists
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Diagnosis
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Diagnosis, Oral
;
Follow-Up Studies
;
Hereditary Sensory and Autonomic Neuropathies
;
Humans
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Hyperesthesia
;
Hypohidrosis
;
Intellectual Disability
;
Pain Insensitivity, Congenital
;
Reflex
;
Sweat
8.Severe Hyperhidrosis in Apert Syndrome: A Case Report
Hanjae LEE ; Sungjun CHOI ; Ji Hoon YANG ; Jungyoon MOON ; Dae Hun SUH
Korean Journal of Dermatology 2019;57(9):548-550
Apert syndrome is a rare genetic disorder characterized by malformations of the skull, face, hands, and feet. We report a case of severe hyperhidrosis in a 13-month-old female infant with Apert syndrome who was born with craniosynostosis, midface hypoplasia, and syndactyly of both hands. She had a history of excessive sweating since birth and this was confirmed using the iodine-starch test. Hyperhidrosis was first reported as a key cutaneous manifestation of Apert syndrome in 1993. However, the main focus in the field of dermatology is on antibiotic-refractory acne, which serves as another cutaneous hallmark of the disease. This is the first report in the Korean literature that describes hyperhidrosis in Apert syndrome. We highlight the presentation of hyperhidrosis as a key cutaneous manifestation in Apert syndrome.
Acne Vulgaris
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Acrocephalosyndactylia
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Craniosynostoses
;
Dermatology
;
Female
;
Foot
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Hand
;
Humans
;
Hyperhidrosis
;
Infant
;
Parturition
;
Skull
;
Sweat
;
Sweating
;
Syndactyly
9.Eccrine porocarcinoma on the cheek
Bommie Florence SEO ; Hyuk Joon CHOI ; Sung No JUNG
Archives of Craniofacial Surgery 2019;20(1):48-50
Eccrine porocarcinoma is a rare malignant tumor arising from the intraepidermal ductal portion of the eccrine sweat gland. It develops either spontaneously or from a long standing benign eccrine poroma. This entity usually affects older people and is commonly located on the lower extremities, the trunk, and the head. We report a case of eccrine porocarcinoma on the left cheek in an 85-year-old male. In our case, the tumor was treated with wide excision and postoperative adjuvant radiation therapy. The patient recovered well without local recurrence and distant metastasis during the 14-month follow-up period. Wide excision and postoperative adjuvant radiation therapy can be considered as a safe and effective treatment option in treating patients with eccrine porocarcinoma.
Aged, 80 and over
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Cheek
;
Eccrine Porocarcinoma
;
Follow-Up Studies
;
Head
;
Humans
;
Lower Extremity
;
Male
;
Neoplasm Metastasis
;
Poroma
;
Radiotherapy, Adjuvant
;
Recurrence
;
Sweat Gland Neoplasms
;
Sweat Glands
10.A case of anhidrotic ectodermal dysplasia presenting with pyrexia, atopic eczema, and food allergy
Tamaho SUZUKI ; Hanako TAJIMA ; Makoto MIGITA ; Ruby PAWANKAR ; Takeshi YANAGIHARA ; Atsushi FUJITA ; Yoshio SHIMA ; Emi YANAI ; Yasuhiko KATSUBE
Asia Pacific Allergy 2019;9(1):e3-
Anhidrotic ectodermal dysplasia (AED) is a rare hereditary disorder with a triad of sparse hair, dental hypoplasia, and anhidrosis. Here we report a case of AED with food allergy and atopic eczema. The patient was a 11-month-old boy admitted to our hospital with pyrexia for 2 weeks. He presented with a history of dry skin, eczema, and food allergy to egg. On clinical examination, his body temperature was 38.8°C, with dry skin and eczema almost all over the body, sparse eyebrows, and scalp hair. Laboratory investigations and physical examination did not show any evidence of infection. Radioallergosorbent test was positive to egg yolk, egg white, ovomucoid, milk, house dust, and house dust mite. As the child did not sweat despite the high fever, we performed the sweat test which revealed a total lack of sweat glands. Genetic examination revealed a mutation of the EDA gene and he was diagnosed as AED. His pyrexia improved upon cooling with ice and fan. His mother had lost 8 teeth and her sweat test demonstrated low sweating, suggestive of her being a carrier of AED. Atopy and immune deficiencies have been shown to have a higher prevalence in patients with AED. Disruption of the skin barrier in patients with AED make them more prone to allergic diseases such as atopic eczema, bronchial asthma, allergic rhinitis and food allergy. Careful assessment of the familial history is essential to differentiate AED when examining patients with pyrexia of unknown origin and comorbid allergic diseases.
Asthma
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Body Temperature
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Child
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Dermatitis, Atopic
;
Dust
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Ectodermal Dysplasia
;
Eczema
;
Egg White
;
Egg Yolk
;
Eyebrows
;
Fever
;
Food Hypersensitivity
;
Hair
;
Humans
;
Hypohidrosis
;
Ice
;
Infant
;
Male
;
Milk
;
Mothers
;
Ovomucin
;
Ovum
;
Physical Examination
;
Prevalence
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Pyroglyphidae
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Radioallergosorbent Test
;
Rhinitis, Allergic
;
Scalp
;
Skin
;
Sweat
;
Sweat Glands
;
Sweating
;
Tooth


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