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  1. Article ; Online: Early Diagnosis of Tuberous Sclerosis Complex: Prenatal Diagnosis.

    Bekiesinska-Figatowska, M / Sobieraj, P / Pasieczna, M / Szymkiewicz-Dangel, J

    AJNR. American journal of neuroradiology

    2023  Volume 44, Issue 9, Page(s) 1070–1076

    Abstract: ... to early diagnosis of tuberous sclerosis complex in many cases. ... detection of tuberous sclerosis complex and the introduction of antiepileptic treatment before seizure onset ... tuberous sclerosis complex sign are detected during fetal ultrasound, and prenatal MR imaging allows detection of cerebral ...

    Abstract Background and purpose: Strong emphasis has been placed recently on early (4 postnatal months) detection of tuberous sclerosis complex and the introduction of antiepileptic treatment before seizure onset. This objective can be achieved prenatally: Cardiac rhabdomyomas and the major diagnostic tuberous sclerosis complex sign are detected during fetal ultrasound, and prenatal MR imaging allows detection of cerebral major manifestations: cortical tubers, subependymal nodules, and subependymal giant cell astrocytomas.
    Materials and methods: We retrospectively reviewed 50 fetuses with ultrasound-detected cardiac tumors at 19-36 gestational weeks (median, 31 weeks). MR imaging with the use of 1.5T scanners was performed at 24-37 gestational weeks (median, 34 weeks).
    Results: In 11 fetuses (22%), cardiac tumors remained the only criterion. In remaining 39 fetuses (78%), MR imaging revealed a prenatal diagnosis of tuberous sclerosis complex, having shown an additional 1-3 major criteria: subependymal nodules in all cases (39/39 = 100.0%), subependymal giant cell astrocytomas in 6 (6/39 = 15.4%), and cortical tubers in 24 (24/39 = 61.5%). Radial migration lines and cerebellar tuber, not published so far, were shown in 1 case each.
    Conclusions: A schedule of proper care of children with tuberous sclerosis complex can be established during the perinatal period due to education of women to report for mandatory ultrasound examinations during pregnancy, the good quality of ultrasound, and referral to MR imaging if a cardiac tumor is depicted on ultrasound. Gynecologists and pediatric cardiologists performing fetal ultrasound and radiologists performing prenatal MR imaging are a key to early diagnosis of tuberous sclerosis complex in many cases.
    MeSH term(s) Child ; Pregnancy ; Humans ; Female ; Tuberous Sclerosis/diagnostic imaging ; Tuberous Sclerosis/therapy ; Retrospective Studies ; Prenatal Diagnosis ; Brain Neoplasms/therapy ; Astrocytoma ; Magnetic Resonance Imaging ; Heart Neoplasms/diagnosis ; Early Diagnosis
    Language English
    Publishing date 2023-08-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 603808-6
    ISSN 1936-959X ; 0195-6108
    ISSN (online) 1936-959X
    ISSN 0195-6108
    DOI 10.3174/ajnr.A7952
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Late diagnosis of tuberous sclerosis: a case report.

    Domínguez-Valdez, Luis F / Hernández-Utrera, Jaime E / Chávez-Sánchez, Iliana N / Peralta-Amaro, Ana L / Talin-Bosquez, Melina J / García-Pedraza, Luis A / Hernández-Jiménez, Carlos A / Delgado-Carmona, Diana K / Gracia-Ramos, Abraham E

    Oxford medical case reports

    2023  Volume 2023, Issue 4, Page(s) omad029

    Abstract: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterized ... usually diagnosed early in life. However, in some cases, the diagnosis is delayed until adulthood ... Confetti-like' skin lesions, shagreen patch), brain (cortical tubers), heart (cardiac rhabdomyomas ...

    Abstract Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder characterized by the formation of hamartomas in organ systems such as the brain, skin, kidneys and lungs. Patients with TSC are usually diagnosed early in life. However, in some cases, the diagnosis is delayed until adulthood because various manifestations occur at various times throughout an individual's life. In this regard, we present the case of a female patient diagnosed at the beginning of the seventh decade of life. The patient had a history of seizures and showed clinical findings on the skin (facial angiofibromas, ungual fibromas, 'Confetti-like' skin lesions, shagreen patch), brain (cortical tubers), heart (cardiac rhabdomyomas), kidneys (angiomyolipomas) and a positive genetic test for mutations in TSC2, fulfilling the diagnostic criteria. We compared the differences between manifestations in patients diagnosed during childhood and adulthood. Knowledge of the clinical spectrum of TSC allows early identification.
    Language English
    Publishing date 2023-04-20
    Publishing country England
    Document type Case Reports
    ZDB-ID 2766251-2
    ISSN 2053-8855
    ISSN 2053-8855
    DOI 10.1093/omcr/omad029
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Prenatal diagnosis of tuberous sclerosis complex

    Neng Jin / Yan Wu / Qing Meng / Qiong Luo

    Heliyon, Vol 9, Iss 6, Pp e16980- (2023)

    Echocardiography, cranial magnetic resonance, and genetic testing of 40 cases with fetal cardiac tumors

    2023  

    Abstract: Objective: To explore the relationship between Tuberous sclerosis complex (TSC) and cardiac tumors ... in the prenatal diagnosis of TSC. Methods: Fetal echocardiography (FE) was performed in the whole population between 2016 ... the diagnosis of TSC can almost be made even without genetic mutation results. ...

    Abstract Objective: To explore the relationship between Tuberous sclerosis complex (TSC) and cardiac tumors at our institution over the past five years and to evaluate the value of imaging technologies and genetic testing in the prenatal diagnosis of TSC. Methods: Fetal echocardiography (FE) was performed in the whole population between 2016 and 2020. Fetuses detected with cardiac tumor(s) were included. Fetal cranial magnetic resonance imaging (MRI) and gene mutation tests were further examined. Those who declined genetic testing were excluded in the final analysis. Results: A total of 40 fetuses were included in our study. There were 27 cases performed cranial magnetic resonance imaging (MRI) and the rest of 13 cases refused. Among 10 fetuses with cranial lesions detected by MRI, all of them were eventually diagnosed with TSC. And for 17 fetuses without cranial lesions, none of them were identified with a pathogenic variation in gene TSC1/2. The prevalence of TSC was significantly higher in the multiple tumors group than in the solitary group (9/20 vs. 2/20, P = 0.034). 11 fetuses had TSC1 (n = 3) or TSC2 (n = 8) causative or suspected causative mutations, of which 9 were sporadic mutations and 2 were familial mutations. Conclusion: Fetal cranial MRI should be recommended to evaluate brain lesions, and genetic mutation should be examined, if possible, especially for those with multiple heart tumors. When typical cardiac tumors and cranial lesions are detected, the diagnosis of TSC can almost be made even without genetic mutation results.
    Keywords Fetal cardiac tumor ; Tuberous sclerosis complex ; Fetal echocardiography ; Genetic testing ; Termination of pregnancy ; Fetal cranial MRI ; Science (General) ; Q1-390 ; Social sciences (General) ; H1-99
    Subject code 610 ; 616
    Language English
    Publishing date 2023-06-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  4. Article: Diagnosis of tuberous sclerosis complex in adulthood: A case report.

    Cruz-Zuniga, Rubén D / Alas-Pineda, César / Pineda-Vijil, Héctor O / Gaitán-Zambrano, Kristhel / Flores-Reyes, Diana L / Pineda-Villeda, Reenie H / Quiñonez-Sánchez, Marco A

    Clinical case reports

    2022  Volume 10, Issue 12, Page(s) e6555

    Abstract: Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder. TSC consists of a wide ...

    Abstract Tuberous sclerosis complex (TSC) is an autosomal dominant genetic disorder. TSC consists of a wide variety of clinical manifestations, with neurological and dermatological symptoms being the most frequent. This study aims to describe the clinical characteristics and management of a pregnant patient incidentally diagnosed with TSC.
    Language English
    Publishing date 2022-12-02
    Publishing country England
    Document type Case Reports
    ZDB-ID 2740234-4
    ISSN 2050-0904
    ISSN 2050-0904
    DOI 10.1002/ccr3.6555
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: How early is too early? Diagnosis of tuberous sclerosis complex in a neonate.

    Prashanth, R R / Nair, S / Haribalakrishna, A / Thakkar, H

    Journal of postgraduate medicine

    2023  Volume 69, Issue 4, Page(s) 243–244

    MeSH term(s) Infant, Newborn ; Humans ; Tuberous Sclerosis/diagnosis ; Brain ; Diagnosis, Differential
    Language English
    Publishing date 2023-09-07
    Publishing country India
    Document type Journal Article
    ZDB-ID 410691-x
    ISSN 0972-2823 ; 0022-3859
    ISSN (online) 0972-2823
    ISSN 0022-3859
    DOI 10.4103/jpgm.jpgm_326_23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Fetal neurosonography as accurate tool for diagnosis of brain involvement in tuberous sclerosis.

    Malinger, G / Prabhu, A / Maroto González, A / Brusilov, M / Kidron, D / Amster, R / Birnbaum, R / Krajden Haratz, K

    Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology

    2023  Volume 62, Issue 3, Page(s) 391–397

    Abstract: ... of fetal brain involvement in tuberous sclerosis complex.: Methods: This was a multicenter ... retrospective study of fetuses at high risk for tuberous sclerosis complex. Dedicated neurosonographic, fetal ... on dedicated imaging. We searched for tuberous sclerosis complex-related brain involvement, defined ...

    Abstract Objective: To demonstrate the potential utility of dedicated neurosonography for the diagnosis of fetal brain involvement in tuberous sclerosis complex.
    Methods: This was a multicenter retrospective study of fetuses at high risk for tuberous sclerosis complex. Dedicated neurosonographic, fetal magnetic resonance imaging (MRI) and postnatal reports were reviewed. Data collected included reason for referral, gestational age at which cardiac rhabdomyoma was first suspected and final number of cardiac rhabdomyomas detected on dedicated imaging. We searched for tuberous sclerosis complex-related brain involvement, defined as the presence of one or more of the following findings: white-matter lesions; subependymal nodules; cortical/subcortical tubers; and subependymal giant-cell astrocytoma.
    Results: We included 20 patients at high risk of tuberous sclerosis complex, of whom 19 were referred for the presence of cardiac rhabdomyomas and one for a deletion in chromosome 16 involving the tuberous sclerosis complex gene locus. Cardiac rhabdomyomas were diagnosed at a mean gestational age of 27 + 2 weeks (range, 16 + 0 to 36 + 3 weeks) and the mean number of cardiac rhabdomyomas per patient was 4 (range, 1-10). Brain involvement was present in 15 fetuses, in 13 of which the disease was confirmed in one or more of the following ways: chromosomal microarray analysis (n = 1), exome sequencing (n = 7), autopsy (n = 4), clinical tuberous sclerosis complex in the newborn (n = 4) and a sibling diagnosed with clinical tuberous sclerosis complex (n = 1). In two cases, the disease could not be confirmed: one was lost to follow-up and autopsy, following termination of pregnancy, was not performed in the other. Among the five cases without brain findings, tuberous sclerosis complex was confirmed in three by exome sequencing (n = 2) and/or autopsy findings (n = 2). The two remaining cases had normal exome sequencing; one case had five cardiac rhabdomyomas, which was a highly suggestive finding, while in the final case, the autopsy was considered normal, representing the only false-positive case in our cohort.
    Conclusions: Contrary to current literature, dedicated neurosonography appears to be effective in the diagnosis of brain involvement in fetuses at risk of tuberous sclerosis complex and should be used as the first-line approach. Although the number of cases in which MRI was performed was small, it seems that, in the presence of ultrasound findings, the added value of MRI is low. © 2023 The Authors. Ultrasound in Obstetrics & Gynecology published by John Wiley & Sons Ltd on behalf of International Society of Ultrasound in Obstetrics and Gynecology.
    MeSH term(s) Pregnancy ; Infant, Newborn ; Female ; Humans ; Infant ; Tuberous Sclerosis/genetics ; Rhabdomyoma/diagnostic imaging ; Rhabdomyoma/pathology ; Retrospective Studies ; Brain/diagnostic imaging ; Brain/pathology ; Fetus/diagnostic imaging ; Fetus/pathology ; Heart Neoplasms/diagnostic imaging ; Heart Neoplasms/genetics
    Language English
    Publishing date 2023-04-04
    Publishing country England
    Document type Multicenter Study ; Journal Article
    ZDB-ID 1073183-0
    ISSN 1469-0705 ; 0960-7692
    ISSN (online) 1469-0705
    ISSN 0960-7692
    DOI 10.1002/uog.26213
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Presentation and diagnosis of neonatal tuberous sclerosis complex: A case report and literature review.

    Karki, Susmin / Bhatta, Pramish / Parajuli, Asmita / Kumari, Khusbu / Rijal, Divas / Harrylal, Kayleigh Anjali / Gautam, Shristi / Sharma, Arun Kumar

    SAGE open medical case reports

    2024  Volume 12, Page(s) 2050313X241252342

    Abstract: Tuberous sclerosis is an uncommon neurocutaneous syndrome characterized by hamartomatous growths ... with unpredictable progression. Diagnosing and managing neonatal tuberous sclerosis can be challenging. We report ... with tuberous sclerosis with multisystem involvement. ...

    Abstract Tuberous sclerosis is an uncommon neurocutaneous syndrome characterized by hamartomatous growths with unpredictable progression. Diagnosing and managing neonatal tuberous sclerosis can be challenging. We report a rare case of a 30-day-old male born out of a non-consanguineous marriage who presented with poor suckling and persistent abnormal body movement, required prolonged intensive care, and was diagnosed with tuberous sclerosis with multisystem involvement.
    Language English
    Publishing date 2024-05-06
    Publishing country England
    Document type Case Reports
    ZDB-ID 2736953-5
    ISSN 2050-313X
    ISSN 2050-313X
    DOI 10.1177/2050313X241252342
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Dermoscopy of hypopigmented macules unveiling genetic diagnosis of tuberous sclerosis complex type 2 in an infant presenting with sacral chordoma.

    Sharma, Ananya / Aggarwal, Bhawana / Kakkar, Aanchal / Pandey, Niraj Nirmal / Taneja, Neha

    Pediatric dermatology

    2024  

    Abstract: ... to a diagnosis of tuberous sclerosis, confirmed with the finding of a heterozygous TSC2 gene deletion; treatment ... These dermoscopic findings were suggestive of the ash-leaf macules of tuberous sclerosis over other common ... reported as a rare manifestation of tuberous sclerosis complex. The combination of these findings led ...

    Abstract A 2-month-old male with surgically resected sacral chordoma presented with multiple hypopigmented macules showing characteristic patchy, sharply demarcated areas of pigment network on dermoscopy. These dermoscopic findings were suggestive of the ash-leaf macules of tuberous sclerosis over other common hypopigmented macules in neonates. Chordomas presenting in early childhood in the sacral location have been reported as a rare manifestation of tuberous sclerosis complex. The combination of these findings led to a diagnosis of tuberous sclerosis, confirmed with the finding of a heterozygous TSC2 gene deletion; treatment with sirolimus resulted in regression of cardiac rhabdomyomas and hypopigmented macules.
    Language English
    Publishing date 2024-03-18
    Publishing country United States
    Document type Letter
    ZDB-ID 605539-4
    ISSN 1525-1470 ; 0736-8046
    ISSN (online) 1525-1470
    ISSN 0736-8046
    DOI 10.1111/pde.15581
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article: Editorial: Tuberous Sclerosis Complex - Diagnosis and Management.

    Jozwiak, Sergiusz / Curatolo, Paolo

    Frontiers in neurology

    2021  Volume 12, Page(s) 755868

    Language English
    Publishing date 2021-10-05
    Publishing country Switzerland
    Document type Editorial
    ZDB-ID 2564214-5
    ISSN 1664-2295
    ISSN 1664-2295
    DOI 10.3389/fneur.2021.755868
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Early diagnosis of a newborn with tuberous sclerosis caused by a genetic mutation.

    Qiao, Lin / Yang, Yuting / Yue, Dongmei

    The Journal of international medical research

    2022  Volume 49, Issue 8, Page(s) 3000605211035895

    Abstract: Objective: Tuberous sclerosis (TSC) is an autosomal dominant disorder, often detected during ...

    Abstract Objective: Tuberous sclerosis (TSC) is an autosomal dominant disorder, often detected during childhood. We present the results of genetic testing in a newborn with suspected TSC.
    Methods: A newborn with no specific clinical manifestations of TSC showed evidence of TSC on magnetic resonance imaging and echocardiography. Next-generation sequencing (NGS) and multiple ligation-dependent probe amplification (MLPA) of the
    Results: The results of MLPA were negative, but NGS showed a heterozygous mutation in the
    Conclusions: In this case, a case of TSC caused by a heterozygous mutation in the
    MeSH term(s) DNA Mutational Analysis ; Early Diagnosis ; Humans ; Infant, Newborn ; Mutation ; Tuberous Sclerosis/diagnostic imaging ; Tuberous Sclerosis/genetics ; Tuberous Sclerosis Complex 1 Protein/genetics ; Tuberous Sclerosis Complex 2 Protein/genetics ; Tumor Suppressor Proteins/genetics
    Chemical Substances TSC1 protein, human ; TSC2 protein, human ; Tuberous Sclerosis Complex 1 Protein ; Tuberous Sclerosis Complex 2 Protein ; Tumor Suppressor Proteins
    Language English
    Publishing date 2022-01-21
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 184023-x
    ISSN 1473-2300 ; 0300-0605 ; 0142-2596
    ISSN (online) 1473-2300
    ISSN 0300-0605 ; 0142-2596
    DOI 10.1177/03000605211035895
    Database MEDical Literature Analysis and Retrieval System OnLINE

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