- Happle-Tinschert Syndrome: A Case Report of Unilateral Segmentally Arranged Basaloid Follicular Hamartoma with Scoliosis and Review of Literature
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Seo SH, Lee SE, Kim SC
- KMID: 2471344
- Ann Dermatol.
- 2020 Apr;32(2):159-163.
- doi: 10.5021/ad.2020.32.2.159
Happle-Tinschert syndrome is a rare disease characterized by unilateral, segmentally arranged basaloid follicular hamartoma (BFH) with osseous, dental, and cerebral anomalies. Although BFH has been demonstrated to be associated with... -
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- Coincidence of Dermal Melanocyte Hamartoma and Becker's Nevus in a Patient with Neurofibromatosis Type 1
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Kim YJ, Choi ME, Lee MW, Choi JH, Chang SE
- KMID: 2470219
- Korean J Dermatol.
- 2019 Dec;57(10):632-634.
Dermal melanocytosis is characterized by an increased number of ovoid to elongated melanocytes situated between collagen fibers in the dermis, including blue nevus, Mongolian spots, nevus of Ota and Ito... -
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- Hair Follicle Nevus Located on the Neck: Comparison with Accessory Tragus, Cervical Chondrocutaneous Branchial Remnants and Trichofolliculoma
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Lee JS, Yang JH, Park H, Yoon HS, Cho S
- KMID: 2461989
- Ann Dermatol.
- 2019 Dec;31(6):662-665.
- doi: 10.5021/ad.2019.31.6.662
Hair follicle nevus (HFN) is a rare, benign, follicular hamartoma that most frequently presents as a congenital nodule on the face. We experienced a rare case of HFN on the... -
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- A Case of Mucinous Gland Adenomatoid Hamartoma Originated from Submental Space
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Kim SW, Lee SM, Lee KH, Park KJ, Park HS
- KMID: 2469238
- Korean J Head Neck Oncol.
- 2019 Nov;35(2):61-65.
- doi: 10.21593/kjhno/2019.35.2.61
Hamartomas are non-neoplastic malformations or congenital errors of tissue development. Hamartoma is composed by an excessive growth of mature tissue present in wrong proportions and abnormal arrangements. The lesion usually... -
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- Three Cases of Nasal Chondromesenchymal Hamartoma Occurred in Sinonasal Tract
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Choi Y, Jang YJ, Cho KJ, Chung YS
- KMID: 2466715
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2019 Nov;62(11):651-656.
- doi: 10.3342/kjorl-hns.2018.00815
Nasal chondromesenchymal hamartoma (NCMH) is a rare benign tumor of the sinonasal tract. Most NCMH has a benign nature and can be cured by complete resection. Only a few NCMH... -
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- Juvenile Polyp associated with Hypovolemic Shock Due to Massive Lower Gastrointestinal Bleeding
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Kim DY, Bae JY, Ko KO, Cheon EJ, Lim JW, Song YH, Yoon JM
- KMID: 2462104
- Pediatr Gastroenterol Hepatol Nutr.
- 2019 Nov;22(6):613-618.
- doi: 10.5223/pghn.2019.22.6.613
Juvenile polyps are the most common types of polyps in children, and patients usually present with lower gastrointestinal (GI) bleeding as the predominant symptom. These lesions, which are referred to... -
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- Use of Topical Rapamycin as Maintenance Treatment after a Single Session of Fractionated COâ‚‚ Laser Ablation: A Method to Enhance Percutaneous Drug Delivery
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Oh J, Kim J, Lee WJ, Lee JH
- KMID: 2456233
- Ann Dermatol.
- 2019 Oct;31(5):555-558.
- doi: 10.5021/ad.2019.31.5.555
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder with an incidence of approximately 1 in 5,000 to 10,000 live births. TSC has various clinical manifestations such as multiple... -
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- A Case of Post-Herpetic Nevoid Comedones
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Seo JK, Jeong KH, Shin MK
- KMID: 2456672
- Ann Dermatol.
- 2019 Aug;31(Suppl):S36-S38.
- doi: 10.5021/ad.2019.31.S.S36
No abstract available. -
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- A Case of Post-Herpetic Nevoid Comedones
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Seo JK, Jeong KH, Shin MK
- KMID: 2456645
- Ann Dermatol.
- 2019 Aug;31(Suppl 1):S36-S38.
- doi: 10.5021/ad.2019.31.S.S36
No abstract available. -
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- A case of pancreatic hamartoma pathologically confirmed after robot-assisted pancreaticoduodenectomy
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Shin DH, Rho SY, Hwang HK, Lee WJ, Kang CM
- KMID: 2456029
- Ann Hepatobiliary Pancreat Surg.
- 2019 Aug;23(3):286-290.
- doi: 10.14701/ahbps.2019.23.3.286
Pancreatic hamartoma is a rare benign tumor that can be easily misdiagnosed due to its rarity. Its diagnostic ambiguity demands surgical resection for confirmation. We reported a 54-year-old female patient... -
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- Cowden Disease: Case Report and Review of the Literature
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Son JH, Chung BY, Jung MJ, Choi YW, Kim HO, Park CW
- KMID: 2444866
- Ann Dermatol.
- 2019 Jun;31(3):325-330.
- doi: 10.5021/ad.2019.31.3.325
Cowden's disease is a rare autosomal dominant, multiple hamartoma syndrome with characteristic mucocutaneous lesions. It is associated with abnormalities of the breast, thyroid, and gastrointestinal tract; and is characterized by... -
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- A Primer on Magnetic Resonance-Guided Laser Interstitial Thermal Therapy for Medically Refractory Epilepsy
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Lee EJ, Kalia SK, Hong SH
- KMID: 2453241
- J Korean Neurosurg Soc.
- 2019 May;62(3):353-360.
- doi: 10.3340/jkns.2019.0105
Epilepsy surgery that eliminates the epileptogenic focus or disconnects the epileptic network has the potential to significantly improve seizure control in patients with medically intractable epilepsy. Magnetic resonance-guided laser interstitial... -
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- Congenital Dermal Melanocytosis on the Foot: A Case Report and Review of the Literature
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Cho SI, Moon J, Jo G, Lee C, Mun JH
- KMID: 2439069
- Ann Dermatol.
- 2019 Apr;31(2):213-216.
- doi: 10.5021/ad.2019.31.2.213
Dermal melanocytosis is a common pigmented skin disease, characterized by an increased number of ectopic melanocytes in the dermis. Rare variants of dermal melanocytosis that do not belong to these... -
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- Episodes of prolonged “trance-like state†in an infant with hypothalamic hamartoma
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Kumar R, Yadav J, Sahu JK, Tripathi M, Ahuja C, Dayal D
- KMID: 2447377
- Ann Pediatr Endocrinol Metab.
- 2019 Mar;24(1):55-59.
- doi: 10.6065/apem.2019.24.1.55
Hypothalamic hamartoma (HH) is one of the most common causes of central precocious puberty (CPP) in first few years of life. It can present with either seizures or CPP, although... -
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- PTEN Mutation Identified in Patient Diagnosed with Simultaneous Multiple Cancers
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Won HS, Chang ED, Na SJ, Whang IY, Lee DS, You SH, Kim YS, Kim JS
- KMID: 2437630
- Cancer Res Treat.
- 2019 Jan;51(1):402-407.
- doi: 10.4143/crt.2017.579
PTEN hamartoma tumor syndrome is a spectrum of disorders characterized by unique phenotypic features including multiple hamartomas caused by mutations of the tumor suppressor gene PTEN. Cowden syndrome and Bannayan–Riley–Ruvalcaba... -
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- Giant complex odontoma in the posterior mandible: A case report and literature review
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Park JC, Yang JH, Jo SY, Kim BC, Lee J, Lee W
- KMID: 2450170
- Imaging Sci Dent.
- 2018 Dec;48(4):289-293.
- doi: 10.5624/isd.2018.48.4.289
Odontomas are considered a type of odontogenic hamartoma, and are generally reported not to exceed 3 cm in diameter. Some authors have referred to odontomas with a diameter exceeding 3... -
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- Tuberous Sclerosis Complex with Crohn's Disease
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Kim MH, Lee YJ, Kim JY, Yi YY, Kang JW
- KMID: 2437115
- J Korean Child Neurol Soc.
- 2018 Dec;26(4):284-287.
- doi: 10.26815/jkcns.2018.26.4.284
Tuberous sclerosis complex (TSC) is an autosomal dominant disorder caused by mutation of one of two genes, TSC1 (encoding hamartin, 9q34) and TSC2 (encoding tuberin, 16p13). It invades the central... -
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- Synchronous Bilateral Breast Carcinoma in a Patient with Cowden Syndrome with PTEN Mutation: A Case Report
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Kwon SY, Yeo SH, Ha JS, Kang SH
- KMID: 2434908
- J Breast Dis.
- 2018 Dec;6(2):79-83.
- doi: 10.14449/jbd.2018.6.2.79
Cowden syndrome (CS), also known as multiple hamartomas syndrome, is a rare hereditary autosomal dominant disorder caused by a germline mutation in the phosphatase and tensin homolog (PTEN) gene mapped... -
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- A Case of Hamartoma of the Subglottis
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Lee MJ, Kim JY, Shim HK, Kim MR
- KMID: 2436511
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2018 Jul;61(7):370-373.
- doi: 10.3342/kjorl-hns.2016.17454
Hamartoma is a developmental anomaly or non-neoplastic malformations composed by an excessive growth of indigenous mature tissue present in wrong proportions and abnormal arrangements. Hamartomas may develop in all areas... -
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- Unilateral rostral mandibulectomy for gingival vascular hamartoma in two calves
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Tsuka T, Okamoto Y, Yamamoto N, Hayashi K, Morita T, Sunden Y, Murahata Y, Azuma K, Osaki T, Ito N, Imagawa T
- KMID: 2417576
- J Vet Sci.
- 2018 Jul;19(4):582-584.
- doi: 10.4142/jvs.2018.19.4.582
A 2-month-old female Holstein calf and a 5-month-old female Japanese black calf presented with gingival vascular hamartoma located in the interdental space between the second and third mandibular incisors in... -
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