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Case Report

Metastasis of Hepatocellular Carcinoma in the Pouch of Douglas Successfully Treated by Radiation Therapy: A Case Report

by
Hirayuki Enomoto
1,*,
Masayuki Fujiwara
2,
Hiroshi Kono
3,
Yasukazu Kako
2,
Motonori Takahagi
2,
Junichi Taniguchi
2,
Eri Ishikawa
3,
Naoto Ikeda
1,
Tomoyuki Takashima
1,
Yukihisa Yuri
1,
Nobuhiro Aizawa
1,
Mamiko Okamoto
1,
Kohei Yoshihara
1,
Ryota Yoshioka
1,
Shoki Kawata
1,
Shogo Ota
1,
Ryota Nakano
1,
Hideyuki Shiomi
1,
Takashi Nishimura
1,
Seiichi Hirota
3,
Koichiro Yamakado
2 and
Hiroko Iijima
1
add Show full author list remove Hide full author list
1
Division of Hepatobiliary and Pancreatic Disease, Department of Internal Medicine, Hyogo Medical University, Mukogawa-cho 1-1, Nishinomiya 663-8501, Hyogo, Japan
2
Department of Radiology, Hyogo Medical University, Nishinomiya 663-8501, Hyogo, Japan
3
Department of Surgical Pathology, Hyogo Medical University, Nishinomiya 663-8501, Hyogo, Japan
*
Author to whom correspondence should be addressed.
Life 2023, 13(1), 225; https://doi.org/10.3390/life13010225
Submission received: 24 October 2022 / Revised: 2 January 2023 / Accepted: 11 January 2023 / Published: 13 January 2023
(This article belongs to the Section Medical Research)

Abstract

:
Metastasis of hepatocellular carcinoma (HCC) in the pouch of Douglas is relatively rare. A 65-year-old man with liver cirrhosis was admitted for detailed examination of a pelvic tumor. He had a previous history of ruptured HCC, and received emergent hemostasis with transcatheter arterial embolization followed by curative ablation. His blood tests showed an increase in des-gamma-carboxy prothrombin (DCP). Contrast-enhanced computed tomography (CE-CT) revealed a heterogeneously enhanced large pelvic tumor, but no additional tumorous lesions were detected in other organs, including the lungs, liver and abdominal lymph nodes. The colonoscopy showed compression by an extra-luminal/submucosal tumor, and computed tomography-guided percutaneous needle biopsy revealed that the pelvic tumor was metastasis of HCC. Because of the poor liver function, the solitary pelvic tumor was treated with three-dimensional conformal radiation therapy (3D-CRT). The tumor size and the DCP value were markedly decreased after radiation therapy. Nine months later, occasional mild bloody stool due to radiation proctitis was observed; however, no serious side effects occurred. Our case suggests that radiation therapy may be a therapeutic option for a solitary metastatic lesion of HCC in the pouch of Douglas.

1. Introduction

Peritoneal dissemination is a relatively rare complication of hepatocellular carcinoma (HCC), which was reported to be observed in 2–15% of HCC cases [1]. Tumor rupture, diaphragmatic invasion, and lymph node metastasis were suggested to be risk factors for peritoneal dissemination [2,3]. No decisive treatment protocol for the disseminated tumor has been established, though systemic chemotherapies could be generally selected as a first-line therapy [4,5]. We herein report a case involving a patient who suffered from a large metastatic lesion of HCC in the pouch of Douglas, which was successfully treated with radiation therapy (RT).

2. Case Report: Successful Radiation Therapy for the Treatment of Metastasis of Hepatocellular Carcinoma in the Pouch of Douglas (Table 1)

A 65-year-old man with liver cirrhosis was admitted to our hospital for the detailed examination of a pelvic tumor. There were no complaints of any particular symptoms, but periodic blood tests showed an increase in the des-gamma-carboxy prothrombin (DCP); however, no liver tumor was found on abdominal ultrasonography. Contrast-enhanced computed tomography (CE-CT) showed a large pelvic tumor (Figure 1). No other tumorous lesions were detected in the other organs, including the liver, lungs, and abdominal lymph nodes. Contrast-enhanced magnetic resonance imaging (CE-MRI) suggested the presence of a malignant tumor (Figure 2).
Table 1. The timeline of the case.
Table 1. The timeline of the case.
YearMonthEvent
X-5 The diagnosis of NASH-related liver cirrhosis
JanuaryRupture of HCC and emergent hemostasis with TAE
X-3MayCurative treatment of the HCC (re-TAE and additional RFA)
(Start of HCC follow-up in our hospital after curative therapy)
MarchIncrease in the DCP and detection of the pelvic tumor
Medical interview revealing mild constipation
XMayThe histological diagnosis of pelvic metastasis of HCC
August–October3D-CRT (prescribed dose for the gross tumor: 60 Gy in 30 fractions)
(Decrease in the tumor size and DCP values, constipation resolved)
X + 1JulyOccasional bloody stool and the diagnosis of radiation proctitis (grade 1) by colonoscopy
HCC: hepatocellular carcinoma; TAE: transcatheter arterial embolization; RFA: radiofrequency ablation; DCP: des-gamma-carboxy prothrombin; 3D-CRT: three-dimensional conformal radiation therapy.
The patient had suffered from diabetes and been diagnosed with liver cirrhosis due to nonalcoholic fatty liver disease. He had a history of ruptured hepatocellular carcinoma (HCC), located near the surface of the right posterior-inferior segment (Segment VI) of the liver, and had undergone emergent hemostasis with transcatheter arterial embolization (TAE). He had also received subsequent radiofrequency ablation for the curative treatment of HCC. When the HCC treatment had been completed, his liver reserve function had shown a decompensated status (Child–Pugh grade B). Because of the patient’s history of ruptured HCC and increased DCP value, we assumed the presence of metastasis in the pouch of Douglas. A medical interview revealed the presence of mild constipation, and the colonoscopy showed a normal rectal mucosa with compression by an extra-luminal tumor (Figure 3). Histological assessment with computed tomography-guided percutaneous needle biopsy revealed that the tumor was metastasis of HCC (Figure 4). He had decompensated cirrhosis (Table 2), and the application of surgical resection or systemic chemotherapy was considered difficult. The large pelvic tumor was the only recurrent lesion that we detected, and we conducted three-dimensional conformal radiation therapy (3D-CRT) with the aim of controlling the metastatic lesion (Figure 5). The prescribed dose for the gross tumor was 60 Gy in 30 fractions, and radiation therapy was successfully completed without any obvious adverse events. The tumor size and DCP value was found to be remarkably decreased (Figure 6 and Figure 7). His liver function did not change after RT for the pelvic tumor, and his constipation was resolved. No severe side effects were observed, although occasional blood stool due to radiation proctitis (grade 1) occurred from approximately 9 months after the completion of RT (Figure 8).

3. Discussion

In Japan, HCC is one of the major malignancies due to the high prevalence of viral hepatitis [6]. Tumor rupture and bleeding is one of the serious complications of HCC, and the incidence is reported to be relatively high in Asia and Africa, ranging from 3 to 26% in HCC patients [7,8]. The mortality rate of patients after the rupture of HCC is reported to be 25–75%; however, the prognosis is suggested to have improved in recent years [7,8,9].
Ruptured lesions are most commonly observed in the left lateral segment (Segments II and III) or right posterior-inferior segment (Segment VI) [10]. Various strategies, such as emergent hepatectomy or TAE are conducted as hemostatic treatment [7]. In the present case, the bleeding occurred in a tumor located in Segment VI, and because of the poor liver reserve function, hemostatic TAE was conducted in another hospital. Therefore, our case showed the typical clinical history of ruptured HCC.
The most unique point in this case was the performance of 3D-CRT for the treatment of metastasis in the pouch of Douglas. Peritoneal dissemination is reported to occur in 2–15% of HCC patients [1]. HCC rupture, diaphragmatic invasion, and lymph node metastasis are reported to be risk factors for peritoneal dissemination [2]. In addition, needle tract seeding due to puncture techniques, including biopsy or percutaneous ablation, has been implicated in peritoneal dissemination [1,2]. The prognostic impact of peritoneal dissemination is unclear, as the progression of the intrahepatic malignant lesions or liver failure would mainly be related to the prognosis in patients with advanced HCC. Recently, systemic treatments for HCC have advanced [11,12] and can be used for patients with extrahepatic lesions [4,5,11,12,13]. However, some reports have suggested that the resection of a disseminated tumor may have beneficial effects on the prognosis [14,15,16]. Some studies have also suggested the clinical utility of cytoreductive surgery in combination with other therapies [17,18]. Therefore, local treatment for a disseminated lesion may be beneficial in certain cases. In our patient, the intrahepatic malignant lesions were well controlled, while the disseminated lesion formed a large tumor. We therefore speculated that the disseminated lesion had the potential to affect the patient’s prognosis. On the other hand, due to the poor hepatic reserve function, neither surgical resection nor systemic chemotherapy appeared to be applicable in our case. The concept of ‘oligometastasis’, which is a clinical state of metastasis with limited metastatic capacity that can be effectively treated with local therapies, has been proposed [19]. The idea has been accepted in various types of solid malignancies and is proposed to be applicable to HCC as well [20]. However, uncertainty concerning the application of such a concept to HCC cases remains, and systemic treatment is still the standard of care for HCC. Our case report may provide some suggestive information and help enhance research regarding “oligometastasis” of HCC.
HCC is known to be sensitive to radiotherapy, and the efficacy of RT has been reported [21,22]. The colonoscopy showed a submucosal tumor without invasion into the lumen (Figure 3), and the risk of perforation was predicted to be low. The disseminated lesion was reduced in size, and the patient’s tumor marker levels were markedly reduced, despite the development of radiation-associated proctitis (grade 1) as a mild side effect. There are few reports on the successful application of RT for the treatment of retroperitoneal metastasis in HCC patients, and to our knowledge, successful RT to treat metastasis of HCC in the pouch of Douglas has not been reported. Our case suggests that RT may be a viable strategy for treating a disseminated lesion in the pouch of Douglas, particularly in cases with a poor hepatic reserve function.
We herein describe a case that was successfully treated with RT. However, several limitations associated with the present study, such as alternative treatments and future applications, warrant mention. The tumor microenvironment in HCC is strongly immunosuppressive, and immunotherapies based on the use of immune checkpoint inhibitors have provided great promise in the treatment of HCC [23,24]. Such new therapies may provide an effective treatment option for this case. In addition, since we obtained the tumor tissue by a percutaneous biopsy, we were able to identify another effective treatment using recently developed technologies, such as cancer genomic profiling [25,26]. Finally, our case report suggests that more precise and individualized approaches need to be tested in well-designed clinical trials. Unfortunately, however, it is not easy for us to propose how our report can lead to such advances in medicine.

4. Conclusions

We experienced a case of HCC metastasis in the pouch of Douglas for which RT was effective. RT might be a viable treatment for metastasis of HCC in the pouch of Douglas, particularly in cases with an insufficient hepatic reserve function.

Author Contributions

All authors contributed to the conception and design of this case report. All authors were involved in data analysis and interpretation. H.E. wrote the first draft of the manuscript. All authors participated in the manuscript revision and approved the manuscript. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

This case report does not require an ethical committee approval.

Informed Consent Statement

Written informed consent has been obtained from the patient to publish this paper.

Data Availability Statement

Data supporting this case report are available from the corresponding author on reasonable request.

Conflicts of Interest

The authors declare no conflict of interest regarding this case report.

References

  1. Da Fonseca, L.G.; Leonardi, P.C.; Hashizume, P.H.; Sansone, F.; Saud, L.R.; Carrilho, F.J.; Herman, P. A multidisciplinary approach to peritoneal metastasis from hepatocellular carcinoma: Clinical features, management and outcomes. Clin. Exp. Hepatol. 2022, 8, 42–48. [Google Scholar] [CrossRef] [PubMed]
  2. Matsukuma, S.; Sato, K. Peritoneal seeding of hepatocellular carcinoma: Clinicopathological characteristics of 17 autopsy cases. Pathol. Int. 2011, 61, 356–362. [Google Scholar] [CrossRef] [PubMed]
  3. Kwak, M.S.; Lee, J.H.; Yoon, J.H.; Yu, S.J.; Cho, E.J.; Jang, E.S.; Kim, Y.J.; Lee, H.S. Risk factors, clinical features, and prognosis of the hepatocellular carcinoma with peritoneal metastasis. Dig. Dis. Sci. 2012, 57, 813–819. [Google Scholar] [CrossRef]
  4. European Association for the Study of the Liver. Electronic address: [email protected]; European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Management of hepatocellular carcinoma. J. Hepatol. 2018, 69, 182–236. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Gordan, J.D.; Kennedy, E.B.; Abou-Alfa, G.K.; Beg, M.S.; Brower, S.T.; Gade, T.P.; Goff, L.; Gupta, S.; Guy, J.; Harris, W.P.; et al. Systemic Therapy for Advanced Hepatocellular Carcinoma: ASCO Guideline. J. Clin. Oncol. 2020, 38, 4317–4345. [Google Scholar] [CrossRef] [PubMed]
  6. Enomoto, H.; Ueno, Y.; Hiasa, Y.; Nishikawa, H.; Hige, S.; Takikawa, Y.; Taniai, M.; Ishikawa, T.; Yasui, K.; Takaki, A.; et al. Transition in the etiology of liver cirrhosis in Japan: A nationwide survey. J. Gastroenterol. 2020, 55, 353–362. [Google Scholar] [PubMed] [Green Version]
  7. Sahu, S.K.; Chawla, Y.K.; Dhiman, R.K.; Singh, V.; Duseja, A.; Taneja, S.; Kalra, N.; Gorsi, U. Rupture of Hepatocellular Carcinoma: A Review of Literature. J. Clin. Exp. Hepatol. 2019, 9, 245–256. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Xia, F.; Ndhlovu, E.; Zhang, M.; Chen, X.; Zhang, B.; Zhu, P. Ruptured Hepatocellular Carcinoma: Current Status of Research. Front. Oncol. 2022, 12, 848903. [Google Scholar] [CrossRef]
  9. Zhu, Q.; Li, J.; Yan, J.J.; Huang, L.; Wu, M.C.; Yan, Y.Q. Predictors and clinical outcomes for spontaneous rupture of hepatocellular carcinoma. World J. Gastroenterol. 2012, 18, 7302–7307. [Google Scholar] [CrossRef]
  10. Li, J.; Huang, L.; Liu, C.F.; Cao, J.; Yan, J.J.; Xu, F.; Wu, M.C.; Yan, Y.Q. Risk factors and surgical outcomes for spontaneous rupture of BCLC stages A and B hepatocellular carcinoma: A case-control study. World J. Gastroenterol. 2014, 20, 9121–9127. [Google Scholar]
  11. Feng, M.Y.; Chan, L.L.; Chan, S.L. Drug Treatment for Advanced Hepatocellular Carcinoma: First-Line and Beyond. Curr. Oncol. 2022, 29, 434. [Google Scholar] [CrossRef] [PubMed]
  12. Llovet, J.M.; Pinyol, R.; Kelley, R.K.; El-Khoueiry, A.; Reeves, H.L.; Wang, X.W.; Gores, G.J.; Villanueva, A. Molecular pathogenesis and systemic therapies for hepatocellular carcinoma. Nat. Cancer 2022, 3, 386–401. [Google Scholar] [CrossRef] [PubMed]
  13. Sonbol, M.B.; Riaz, I.B.; Naqvi, S.A.A.; Almquist, D.R.; Mina, S.; Almasri, J.; Shah, S.; Almader-Douglas, D.; Uson Junior, P.L.S.; Mahipal, A.; et al. Systemic Therapy and Sequencing Options in Advanced Hepatocellular Carcinoma: A Systematic Review and Network Meta-analysis. JAMA. Oncol. 2020, 6, e204930. [Google Scholar] [CrossRef] [PubMed]
  14. Chow, K.C.; Tang, C.N.; Lai, E.C.; Li, M.K. Curative treatment for recurrent tumour implantation after ruptured hepatocellular carcinoma. Hong Kong Med. J. 2013, 19, 82–84. [Google Scholar] [PubMed]
  15. Fang, J.Z.; Yang, Y.; Zhu, H.D.; Sun, J.N.; Mi, H.C.; Lu, C.D. Surgical Treatment of Postoperative Abdominal Metastases of Hepatocellular Carcinoma: 10-Year Experience in a Single Center. Cancer Manag. Res. 2021, 13, 8673–8683. [Google Scholar] [CrossRef] [PubMed]
  16. Iida, H.; Tani, M.; Aihara, T.; Hasegawa, K.; Eguchi, H.; Tanabe, M.; Yamamoto, M.; Yamaue, H. New metastasectomy criteria for peritoneal metastasis of hepatocellular carcinoma: A study of the Japanese Society of Hepato-Biliary-Pancreatic Surgery. Hepatobiliary Pancreat. Sci. 2020, 27, 673–681. [Google Scholar] [CrossRef]
  17. Hung, K.C.; Yang, K.L.; Huang, G.C.; Chen, Y.F.; Chang, W.T.; Chuang, C.C. Cytoreduction surgery and hyperthermic intraperitoneal chemotherapy for treating advanced peritoneal metastases of hepatocellular carcinoma. Pleura Peritoneum 2020, 5, 20190030. [Google Scholar]
  18. Chua, T.C.; Morris, D.L. Exploring the role of resection of extrahepatic metastases from hepatocellular carcinoma. Surg. Oncol. 2012, 21, 95–101. [Google Scholar] [CrossRef]
  19. Weichselbaum, R.R.; Hellman, S. Oligometastases revisited. Nat. Rev. Clin. Oncol. 2011, 8, 378–382. [Google Scholar] [CrossRef]
  20. Kim, K.; Kim, T.H.; Kim, T.H.; Seong, J. Efficacy of Local Therapy for Oligometastatic Hepatocellular Carcinoma: A Propensity Score Matched Analysis. J. Hepatocell. Carcinoma 2021, 8, 35–44. [Google Scholar] [CrossRef]
  21. Lewis, S.; Dawson, L.; Barry, A.; Stanescu, T.; Mohamad, I.; Hosni, A. Stereotactic body radiation therapy for hepatocellular carcinoma: From infancy to ongoing maturity. JHEP. Rep. 2022, 4, 100498. [Google Scholar] [CrossRef] [PubMed]
  22. Rim, C.H.; Seong, J. Application of radiotherapy for hepatocellular carcinoma in current clinical practice guidelines. Radiat. Oncol. J. 2016, 34, 160–167. [Google Scholar] [CrossRef] [PubMed]
  23. Leone, P.; Solimando, A.G.; Fasano, R.; Argentiero, A.; Malerba, E.; Buonavoglia, A.; Lupo, L.G.; De Re, V.; Silvestris, N.; Racanelli, V. The Evolving Role of Immune Checkpoint Inhibitors in Hepatocellular Carcinoma Treatment. Vaccines 2021, 9, 532. [Google Scholar] [CrossRef] [PubMed]
  24. Solimando, A.G.; Susca, N.; Argentiero, A.; Brunetti, O.; Leone, P.; De Re, V.; Fasano, R.; Krebs, M.; Petracci, E.; Azzali, I.; et al. Second-line treatments for Advanced Hepatocellular Carcinoma: A Systematic Review and Bayesian Network Meta-analysis. Clin. Exp. Med. 2022, 22, 65–74. [Google Scholar] [CrossRef] [PubMed]
  25. Yoshii, Y.; Okazaki, S.; Takeda, M. Current Status of Next-Generation Sequencing-Based Cancer Genome Profiling Tests in Japan and Prospects for Liquid Biopsy. Life 2021, 11, 796. [Google Scholar] [CrossRef]
  26. Tsumura, T.; Doi, K.; Marusawa, H. Precision Medicine of Hepatobiliary and Pancreatic Cancers: Focusing on Clinical Trial Outcomes. Cancers 2022, 14, 3674. [Google Scholar] [CrossRef]
Figure 1. Computed tomography (CT) findings. (a) A large pelvic mass of heterogeneous density was detected by plain CT (arrows). (b) The pelvic tumor was mildly enhanced on contrast-enhanced CT.
Figure 1. Computed tomography (CT) findings. (a) A large pelvic mass of heterogeneous density was detected by plain CT (arrows). (b) The pelvic tumor was mildly enhanced on contrast-enhanced CT.
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Figure 2. Findings of magnetic resonance imaging (MRI). The pelvic tumor was shown as a hypo-intensity mass both on T1-weighted imaging (a) and on T2-weighted imaging (b). The tumor showed mild enhancement (c), and was detected as a high-intensity lesion on diffusion-weighted imaging (DWI) (d). The tumor included heterogeneous lesions, presumably showing necrotic tissue with internal bleeding (arrowheads).
Figure 2. Findings of magnetic resonance imaging (MRI). The pelvic tumor was shown as a hypo-intensity mass both on T1-weighted imaging (a) and on T2-weighted imaging (b). The tumor showed mild enhancement (c), and was detected as a high-intensity lesion on diffusion-weighted imaging (DWI) (d). The tumor included heterogeneous lesions, presumably showing necrotic tissue with internal bleeding (arrowheads).
Life 13 00225 g002
Figure 3. Findings of colonoscopy before radiation therapy. Rectal compression by an extra-luminal tumor was observed, but the tumor did not invade the rectal lumen.
Figure 3. Findings of colonoscopy before radiation therapy. Rectal compression by an extra-luminal tumor was observed, but the tumor did not invade the rectal lumen.
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Figure 4. Histological findings of the pelvic tumor. (a,b) Hematoxylin and Eosin staining. (a) A low magnification view of a tumor tissue specimen (×40). (b) A high magnification (×400) view of the boxed area in (a). The proliferation of malignant cells with acidophilic cytoplasm were observed. (cf) Immunostaining of tumor tissue was positive for HepPar-1 (c), HSP70 (d) and Arginase-1 (e). However, in agreement with the blood test results (Table 1), immunostaining of α-fetoprotein was negative (f). Bars, 500 μm (a) and 50 μm (bf).
Figure 4. Histological findings of the pelvic tumor. (a,b) Hematoxylin and Eosin staining. (a) A low magnification view of a tumor tissue specimen (×40). (b) A high magnification (×400) view of the boxed area in (a). The proliferation of malignant cells with acidophilic cytoplasm were observed. (cf) Immunostaining of tumor tissue was positive for HepPar-1 (c), HSP70 (d) and Arginase-1 (e). However, in agreement with the blood test results (Table 1), immunostaining of α-fetoprotein was negative (f). Bars, 500 μm (a) and 50 μm (bf).
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Figure 5. Treatment design of three-dimensional conformal radiation therapy (3D-CRT) for the metastatic tumor in the pouch of Douglas.
Figure 5. Treatment design of three-dimensional conformal radiation therapy (3D-CRT) for the metastatic tumor in the pouch of Douglas.
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Figure 6. Before radiation therapy (RT), a large mass of heterogeneous density was observed ((a): Axial image and (b): Coronal image) (arrowheads). At three months after the completion of RT, the metastatic pelvic tumor was decreased in size ((c): Axial image and (d): Coronal image). The mass reduction was observed at the six months after the completion of the RT ((e): Axial image and (f): Coronal image).
Figure 6. Before radiation therapy (RT), a large mass of heterogeneous density was observed ((a): Axial image and (b): Coronal image) (arrowheads). At three months after the completion of RT, the metastatic pelvic tumor was decreased in size ((c): Axial image and (d): Coronal image). The mass reduction was observed at the six months after the completion of the RT ((e): Axial image and (f): Coronal image).
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Figure 7. The transition in the des-gamma-carboxy prothrombin (DCP) values. The DCP value showed a marked decrease after radiation therapy (RT). The prescribed dose for the gross tumor was 60 Gy in 30 fractions (fr).
Figure 7. The transition in the des-gamma-carboxy prothrombin (DCP) values. The DCP value showed a marked decrease after radiation therapy (RT). The prescribed dose for the gross tumor was 60 Gy in 30 fractions (fr).
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Figure 8. Colonoscopy findings at 9 months after radiation therapy (RT). Radiation-associated proctitis findings, including, telangiectasia, edema, erythema, and bleeding were observed.
Figure 8. Colonoscopy findings at 9 months after radiation therapy (RT). Radiation-associated proctitis findings, including, telangiectasia, edema, erythema, and bleeding were observed.
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Table 2. The laboratory findings of the case.
Table 2. The laboratory findings of the case.
WBC2780/μL(4000–9000)T-bil1.6mg/dL(0.2–1.2)PT-INR1.28 (0.91–1.14)
RBC320×104/μL(410–550)AST61U/L(13–30)PT%62.9%(70–120)
Hb11.2g/dL(13.0–17.0)ALT57U/L(10–42) (46–260)
Hct33.3%(35.0–51.0)ALP197U/L(38–113)HBsAg(-) (-)
Plt88×103/μL(150–350)γ-GTP23U/L(13–64)HBsAb(-) (-)
Alb2.3g/dL(4.1–5.1)HCVAb(-) (-)
Na137mmol/L(138–145)NH3146μg/dL(12–66)
K4.0mmol/L(3.6–4.8) CEA5.6ng/mL(≤5.0)
Cl108mmol/L(101–108)BS180mg/dL(70–109)CA19–916.3U/mL(≤37.0)
BUN14mg/dL(8–20)HbA1c4.8%(4.6–6.2)AFP2.9ng/mL(≤10.0)
CRE0.73mg/dL(0.65–1.07)CRP0.29mg/dL(≤0.3)DCP1950 mAU/mL(<40)
CRE: creatinine, ALP: alkaline phosphatase, γ-GTP: γ-glutamyl transpeptidase, BS: blood sugar, CRP: C-reactive protein, CEA: carcinoembryonic antigen, CA19-9: carbohydrate antigen 19-9, AFP: α-fetoprotein, DCP: des-gamma-carboxy prothrombin.
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MDPI and ACS Style

Enomoto, H.; Fujiwara, M.; Kono, H.; Kako, Y.; Takahagi, M.; Taniguchi, J.; Ishikawa, E.; Ikeda, N.; Takashima, T.; Yuri, Y.; et al. Metastasis of Hepatocellular Carcinoma in the Pouch of Douglas Successfully Treated by Radiation Therapy: A Case Report. Life 2023, 13, 225. https://doi.org/10.3390/life13010225

AMA Style

Enomoto H, Fujiwara M, Kono H, Kako Y, Takahagi M, Taniguchi J, Ishikawa E, Ikeda N, Takashima T, Yuri Y, et al. Metastasis of Hepatocellular Carcinoma in the Pouch of Douglas Successfully Treated by Radiation Therapy: A Case Report. Life. 2023; 13(1):225. https://doi.org/10.3390/life13010225

Chicago/Turabian Style

Enomoto, Hirayuki, Masayuki Fujiwara, Hiroshi Kono, Yasukazu Kako, Motonori Takahagi, Junichi Taniguchi, Eri Ishikawa, Naoto Ikeda, Tomoyuki Takashima, Yukihisa Yuri, and et al. 2023. "Metastasis of Hepatocellular Carcinoma in the Pouch of Douglas Successfully Treated by Radiation Therapy: A Case Report" Life 13, no. 1: 225. https://doi.org/10.3390/life13010225

APA Style

Enomoto, H., Fujiwara, M., Kono, H., Kako, Y., Takahagi, M., Taniguchi, J., Ishikawa, E., Ikeda, N., Takashima, T., Yuri, Y., Aizawa, N., Okamoto, M., Yoshihara, K., Yoshioka, R., Kawata, S., Ota, S., Nakano, R., Shiomi, H., Nishimura, T., ... Iijima, H. (2023). Metastasis of Hepatocellular Carcinoma in the Pouch of Douglas Successfully Treated by Radiation Therapy: A Case Report. Life, 13(1), 225. https://doi.org/10.3390/life13010225

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