Xin He
Zi-Wen Guo
Xiao-Min Niu- Department of Hematology, Zhongshan People’s Hospital, Zhongshan, China
Diffuse hemangiomatosis of the liver and spleen is rare. Currently, few studies are available on diffuse hepatic and splenic hemangiomatosis accompanied by Kasabach–Merritt syndrome (KMS). The conserved telomere maintenance component 1 (CTC1) gene contributes to telomere maintenance and replication by forming the telomeric capping complex. Herein, we report a case of diffuse hemangiomatosis in the liver and spleen accompanied by KMS in a 59-year-old woman who carried two novel heterozygous CTC1 variants: c.435+9A>C and c.3074C>T (p.Ala1025Val). Using next-generation sequencing, we detected mutations in the CTC1 gene in our patient, who had chief complaints of fatigue and abdominal distension complicated by severe thrombocytopenia and consumptive coagulopathy. Clinical symptoms, laboratory tests, and imaging findings led to the diagnosis of diffuse hepatic and splenic hemangiomatosis accompanied by KMS. The patient was treated with prednisone, thalidomide, and sirolimus, and her general condition was ameliorated at the 4-month follow-up with improved platelet count and coagulation function. A CTC1 gene mutation may be involved in the pathological process of vascular diseases. A combination treatment regimen of prednisone, thalidomide, and sirolimus may be effective for KMS.
Introduction
Diffuse hemangiomatosis of the liver and spleen is an extremely rare disease in adults (1). Although most hepatic hemangiomas are benign, they can be fatal when accompanied by Kasabach–Merritt syndrome (KMS), which usually presents as thrombocytopenia, hemolytic anemia, and consumption coagulopathy (2). The conserved telomere maintenance component 1 (CTC1) gene contributes to telomere maintenance, replication, and genetic stability by forming the telomeric capping complex (3). CTC1 gene mutations have been shown to cause cerebroretinal microangiopathy with calcifications and cysts (CRMCC), an autosomal recessive disorder, and dyskeratosis congenita (DC), a telomere biology disorder (4). Additionally, the CTC1 gene has been found to be expressed in endothelial cells (5). CTC1 gene mutations in diffuse hepatic hemangiomas accompanied by KMS remain unreported.
Case presentation
A 59-year-old woman who presented with abdominal distension, fatigue, and skin ecchymosis was referred to our hospital on 12 April 2022. From the medical history, we discovered that the patient experienced asthenia and abdominal distension 1 month previously, and jaundice and skin ecchymoses were exhibited 1 week later. She denied having any other medical or family history or a history of any drug use. Laboratory tests at the local hospital showed anemia, thrombocytopenia, prolonged prothrombin time, hypofibrinogenemia, and hyperbilirubinemia. A fluorodeoxyglucose positron emission tomography (FDG-PET) scan at the local hospital revealed diffuse hepatomegaly and splenomegaly with a slight increase in FDG uptake. Other metabolic abnormalities or intracranial lesions, such as leukoencephalopathy, parenchymal cysts, and intracranial calcification, were not observed (Figure 1). The patient’s condition worsened despite receiving a blood transfusion and expected treatment. Diffuse hepatomegaly, splenomegaly, and ecchymoses without cutaneous hemangioma or neurological disorders were detected during the physical examination. Further examinations, including blood tests and enhanced magnetic resonance imaging (MRI), were performed when the patient was referred to our hospital. Detailed patient characteristics are shown in Table 1.
Figure 1 (A–E) Fluorodeoxyglucose positron emission tomography (FDG-PET) scan performed at the local hospital. The images showed diffuse hepatomegaly and splenomegaly with a slightly increased FDG uptake, without other abnormal FDG accumulation or intracranial lesions. (F–M) A magnetic resonance imaging scan of the abdomen revealed hepatosplenomegaly with countless nodules of various sizes involving the whole liver and spleen, which showed hypointensity on T1-weighted (T1W) images (F), hyperintensity on T2-weighted (T2W) images (G), and inhomogeneous enhancement in diffusion MRI (I, H, L). Diffusion-weighted imaging (DWI) (I) showed a slightly higher signal intensity; however, the apparent diffusion coefficient (ADC) (J) value did not decrease. (F) T1W image. (G) Fat-saturated T2-weighted sequence (fsT2W). (H) The enhanced scan in the transverse view. (I) DWI. (J) ADC. (K) T2W image in the coronal view. (L) The enhanced scan in coronal view. (M) The enhanced scan of the whole abdomen in coronal view.
Table 1 Clinical characteristics of the patient.
Laboratory findings revealed the following abnormalities: White blood cell count, 5.33 (4.0–10.0) × 109/L; hemoglobin, 58 (113–151) g/L; platelet, 9 (101–320) × 109/L; aspartate transaminase, 84 (13–35) U/L; alanine transaminase, 67 (7–40) U/L; total bilirubin, 122.1 (2.0–20.4) μmol/L; direct bilirubin, 61.2 (0–6.8) μmol/L; albumin, 37.2 (40–55) g/L; prothrombin time, >100 (9.0–12.5) s; activated partial thromboplastin time, 35.2 (25.2–38.5) s; fibrinogen, 0.37 (2.0–4.0) g/L; fibrinogen degradation product, 278.4 (0–5) mg/L; international normalized ratio, >8.55 (0.8–1.2); d-dimer, 101.66 (0–0.50) mg/L; α-fetoprotein, 2.0 (<8.1) ng/ml; carbohydrate antigen, 19–9, 9.9 (0–37) U/ml; and carcinoembryonic antigen, 1.0 (0–5.0) ng/ml (Supplementary Table S1). Anti-hepatitis B antigen and anti-hepatitis C antibody tests were negative. Hemolytic tests, including glucose 6-phosphate dehydrogenase activity and Coombs, were normal. The autoantibody profiles, including anti-dsDNA, antinuclear, anti-histone, and anti-SSA antibodies, were negative. DNA tests for Epstein–Barr virus and cytomegalovirus were negative. The MRI showed hepatosplenomegaly with numerous variable-sized nodules in the whole liver and spleen, which showed hypointensity on T1-weighted images and hyperintensity on T2-weighted images and inhomogeneous enhancement in diffusion MRI (Figure 1). Bone marrow aspiration showed reactive bone marrow proliferation, and peripheral blood smear showed fragments of red blood cells. Due to her poor clinical condition, the patient could not cooperate with the liver biopsy. Finally, the clinical symptoms, laboratory tests, and imaging findings led to a diagnosis of diffuse hepatic and splenic hemangiomatosis with KMS. Peripheral blood samples were used to perform whole exome sequencing (WES, The Beijing Genomics Institute, Shenzhen), and the results showed compound heterozygous variants of the CTC1 gene with a missense mutation, c.3074C>T (p.Ala1025Val) (exon 19), and a splicing site mutation, c.435+9A>C (IVS3) (Figure 2). The pathogenicity of both mutations remains unknown. Embolization and surgery could not be performed because of the extensive lesion. After multidisciplinary discussions, the patient was treated with prednisone, 60 mg/day (reduced gradually after 3 weeks); thalidomide, 100 mg/day; and sirolimus, 1 mg/day. She was discharged 2 days after receiving the medications at her and her family’s request. After discharge, the patient returned to her hometown and continued the medications as prescribed. Due to the coronavirus disease 2019 (COVID-19) epidemic, the patient failed to make regular outpatient visits. Through telephonic follow-up, we found that the patient’s abdominal distension and fatigue were reduced, and the ecchymosis had disappeared after 1 month of treatment, while blood checks were not performed this time. After 2 months of taking the medications, the patient had a platelet count of 20 × 109/L and a fibrinogen level of 1.0 g/L. Her anemia, thrombocytopenia, and coagulation function gradually improved 4 months later. Laboratory tests revealed the following: leukocyte count, 6.8 × 109/L; hemoglobin, 90 g/L; platelets, 35 × 109/L; prothrombin time, 13 s; activated partial thromboplastin time, 30 s; and fibrinogen, 1.6 g/L. Although her condition improved, the patient did not consent to CT/MRI review. No significant treatment-related side effects were observed. Relevant clinical courses are shown in Figure 3.
Figure 2 Results of whole exome sequencing showed compound heterozygous variants in the CTC1 gene with a c.3074C>T (p.Ala1025Val) mutation (exon 19) (A) and a c.435+9A>C mutation (IVS3) (B). (A) CTC1 NM_025099.5 exon 19 c.3074C>T (p.Ala1025Val). (B) CTC1 NM_025099.5 IVS3 c.435+9A>C.
Figure 3 Timeline. FDG-PET, fluorodeoxyglucose positron emission tomography.
The patient provided written informed consent for her data to be used in this study, which was approved by the ethics committee of our institution in line with the tenets of the Declaration of Helsinki.
Discussion
Liver hemangiomas, the most common benign liver tumor, can be asymptomatic; however, when the hemangiomas are giant or diffuse, various complications can occur (6). Due to the rarity of adult diffuse hepatic hemangiomatosis, available knowledge is limited and derived mostly from case reports. Diffuse hemangiomatosis occurs in the liver and extrahepatic organs, including the spleen, pancreas, or colon (1, 7). MRI is the most sensitive method for diagnosing hepatic hemangiomas and shows high signal intensity on T2-weighted images with gradual enhancement, which is important for assessing extrahepatic involvement (8). Herein, we report a case of adult diffuse hemangiomatosis of the liver and spleen, which was complicated by severe thrombocytopenia, microangiopathic hemolytic anemia, and consumptive coagulopathy, a lethal condition known as KMS (9, 10).
Hemangiomatosis is a vascular abnormality with an unknown etiology. Etiologic links have been reported between hemangiomatosis and inherited systemic diseases, such as Rendu–Osler–Weber disease and skeletal hemangiomatosis, and between hemangiomatosis and the use of medications, such as metoclopramide and estrogen (11, 12). The correlation between hypothyroidism and diffuse hepatic hemagiomatosis has been described in infants but not in adults (13). In our case, the patient denied any medical history or history of metoclopramide and estrogen intake. Whole exome sequencing was performed to explore the etiology, which revealed compound heterozygous variants of the CTC1 gene: a splicing site mutation, c.435+9A>C, and a novel missense mutation, c.3074C>T (p.Ala1025Val). The CTC1 gene facilitates proper telomere replication and is associated with telomere biology disorders; it has been proven to be relevant in two traditional telomeropathies, CRMCC and DC (14). The main clinical manifestations of CRMCC are retinal telangiectasia and exudation, leukoencephalopathy, parenchymal cysts, and intracranial calcification. Our patient had no ophthalmological and neurological manifestations, and the PET-CT did not show remarkable neuroimaging features of CRMCC, which excluded the diagnosis of CRMCC with later onset. The main clinical features of DC are nail dystrophy, leukoplakia, reticular pigmentation, and bone marrow failure (15). Moreover, the pathogenic variation of CTC1 has been reported to be associated with abnormal manifestations of progeria complicated by recurrent fractures (3). Compared with DC patients, the risk of alimentary tract hemorrhage is higher in patients with CRMCC due to hemangiectasis, which has a higher proportion of CTC1 gene mutations (16). The specific mechanism of CRMCC-related gastrointestinal bleeding remains unclear. However, endoscopy reveals a high proportion of angiectasis in these patients. A mutation in the CTC1 gene may be involved in the pathological process of vascular diseases (17). Hemangiomatosis is considered an angiogenesis or malformation, modulated by many factors; whether the CTC1 gene mutations are involved remains unknown.
Owing to the rarity of the disease, most KMS studies are on neonates and infrequently involve adults. The pathological process of KMS involves the activation and capture of platelets and coagulation factors by the vascular lesions, which causes thrombocytopenia, disseminated intravascular coagulation, and even massive hemorrhage. Vascular lesions correlated with KMS include giant vascular tumors, vascular malformations, and vascular fistulas (18). Furthermore, immune activation, cytokines, and inflammation are considered important contributors to promoting the progression of KMS (19).
The treatment of KMS is challenging. The main goal of therapy is to relieve symptoms and rapidly reduce bleeding. As platelet transfusion can worsen the condition, it is only recommended in emergencies. Surgical management, endovascular intervention, and radiation have been proven to be effective, especially for KMS resulting from a single lesion (20). For diffuse hemangiomatosis with KMS, radiotherapy, endovascular interventional embolization, and other medications did not show significant efficacy. Liver transplantation was considered a radical treatment for diffuse hepatic hemangioma and did not apply to cases with extrahepatic lesions (1). To date, no standard therapeutic guidelines are available for KMS; several therapies, such as vincristine, glucocorticoids, thalidomide, sirolimus, and antivascular endothelial growth factor agents, have been applied in the treatment of KMS (21). Ultimately, our patient received a combination regimen of prednisone, sirolimus, and thalidomide, which led to an improvement. Compared with KMS resulting from a single lesion or cutaneous hemangioma, the response to medications in diffuse hemangiomatosis with KMS is worse (12). The improvement of our patient’s platelet count and coagulation function did not reach the expected level after receiving combined therapy, which may be due to diffuse liver infiltration and extrahepatic lesions. For diffuse hemangiomatosis with KMS, more clinical studies are required to explore the best therapeutic regimen.
In conclusion, we report a case of diffuse hemangiomatosis in the liver and spleen complicated by KMS in a 59-year-old woman who carried two novel heterozygous CTC1 gene variants. Further investigation is required to determine the link between the CTC1 gene mutations and hemangiomatosis. For KMS associated with diffuse hemangiomatosis, which is considered inoperable, a combined regimen of prednisone, sirolimus, and thalidomide can improve survival.
Patient perspective
I began to feel abdominal distension and fatigue, which gradually worsened; it was difficult for me to even eat. I received blood and FDG-PET examinations at a nearby hospital, but the diagnosis was still not precise. After blood transfusions and other treatments, my symptoms became worse. Later, I visited this hospital with my daughter. After careful examinations and multidisciplinary discussions, they gave me a treatment plan. After understanding the severity and rarity of my condition, I hoped to spend more time with my family. I returned to my hometown and continued the medications as prescribed. Over the past few months, my condition has gradually improved.
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found in the article/Supplementary Material.
Ethics statement
Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.
Author contributions
XH wrote the manuscript. ZW,G and XM,N reviewed and edited the manuscript. All authors contributed to the article and approved the submitted version.
Acknowledgments
The authors thank all members of the study team and the patient and her family.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2023.1087790/full#supplementary-material
Supplementary Table 1 | Laboratory data on admission.
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Keywords: diffuse hepatic hemangiomatosis, adult Kasabach-Merritt syndrome, CTC1 gene, combination therapy, vascular disorder
Citation: He X, Guo Z-W and Niu X-M (2023) Case Report: CTC1 mutations in a patient with diffuse hepatic and splenic hemangiomatosis complicated by Kasabach–Merritt syndrome. Front. Oncol. 13:1087790. doi: 10.3389/fonc.2023.1087790
Received: 02 November 2022; Accepted: 10 January 2023;
Published: 25 January 2023.
Edited by:
Jianxun J. Song, Texas A&M Health Science Center, United StatesReviewed by:
Guangfu Li, University of Missouri, United StatesJugal Das, Texas A&M University, United States
Copyright © 2023 He, Guo and Niu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xiaomin Niu, nxm9275@163.com