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DOI:10.2214/AJR.04.1041
AJR 2005; 185:1011-1014
© American Roentgen Ray Society


Case Report

Distended Thoracic Duct and Diffuse Lymphangiectasia Caused by Bancroftian Filariasis

Peter J. Ahn1, Reono Bertagnolli1, Susan L. Fraser2 and Judy H. Freeman3

1 Department of Radiology, Tripler Army Medical Center, 1 Jarrett White Rd., Honolulu, HI 96859.
2 Department of Internal Medicine, Tripler Army Medical Center, Honolulu, HI.
3 Department of Pathology, Tripler Army Medical Center, Honolulu, HI.

Received June 30, 2004; accepted after revision October 15, 2004.

 
The opinions and assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the Department of the Army or the Department of Defense. 1 Jarrett White Rd., Honolulu, HI 96859. Address correspondence to P. J. Ahn (Peter.Ahn{at}andrews.af.mil).


Introduction
Top
Introduction
Case Report
Discussion
References
 
Filariasis is a disease endemic to subtropical areas that is rarely encountered in North America. Because this infection rarely occurs in the United States, our knowledge of CT and MRI findings associated with it is limited. To date, the CT and MRI features of filarial lymphangiectasia in a human have not been described. We present a case of diffuse lymphangiectasia in a patient with filariasis as revealed by CT and MRI findings.



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Fig. 1A 23-year-old man with filariasis. Contrast-enhanced CT scans of chest reveal low-density tubular structure (arrowheads) in posterior mediastinum, with central attenuation value ranging from 15 to 32 H.

 



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Fig. 1B 23-year-old man with filariasis. Contrast-enhanced CT scans of chest reveal low-density tubular structure (arrowheads) in posterior mediastinum, with central attenuation value ranging from 15 to 32 H.

 

Case Report
Top
Introduction
Case Report
Discussion
References
 
A 23-year-old U.S. marine, who was born and raised in Guyana, South America, before emigrating to the United States at age 21, presented to a primary care facility in Japan, his military duty station, with fever and acute abdominal pain radiating to the right groin. Bilateral inguinal adenopathy was found, and a whole-body CT scan revealed what was thought to be diffuse posterior mediastinal, retroperitoneal, pelvic, and inguinal lymphadenopathy. He had no scrotal abnormalities. His symptoms improved on empiric antibiotic therapy, and fine-needle aspiration of an enlarged right inguinal lymph node was performed. He was then referred to our institution with a diagnosis of possible lymphoma.



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Fig. 1C 23-year-old man with filariasis. Single-shot fast spin-echo images (TR/TE, 12,630/99) show tubular structure filled with fluid of high T2 signal intensity.

 



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Fig. 1D 23-year-old man with filariasis. Single-shot fast spin-echo images (TR/TE, 12,630/99) show tubular structure filled with fluid of high T2 signal intensity.

 



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Fig. 1E 23-year-old man with filariasis. Coronal (E) and rotated oblique coronal (F) single-shot fast spin-echo images (11,430/98) further help delineate distended thoracic duct (arrowheads), originating below diaphragm and coursing superiorly just anterior to thoracic vertebral column.

 



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Fig. 1F 23-year-old man with filariasis. Coronal (E) and rotated oblique coronal (F) single-shot fast spin-echo images (11,430/98) further help delineate distended thoracic duct (arrowheads), originating below diaphragm and coursing superiorly just anterior to thoracic vertebral column.

 
Enhanced CT scans of the chest, abdomen, and pelvis were obtained at our institution. The chest CT scan revealed a low-density tubular structure in the posterior mediastinum, with maximum dimensions of 3.0 x 1.6 cm at the T10 level (Figs. 1A and 1B). It extended from the thoracic inlet to the level below the diaphragmatic crura. Single-shot fast spin-echo MR images in multiple planes confirmed a fluid-filled tubular structure extending from L1 level to the junction of left subclavian and internal jugular veins (Figs. 1C, 1D, 1E, and 1F), consistent with a distended thoracic duct. No chylothorax was present. CT of the abdomen revealed diffuse nonenhancing low-density material in the retroperitoneum, surrounding the inferior vena cava, aorta, and proximal renal vessels (Fig. 1G). Similar low-density material was distributed in the pelvis, more prominently along the right iliac vessels (Fig. 1H). MR images confirmed nonenhancing fluid-filled structures distributed in the retroperitoneum and pelvis (Figs. 1I and 1J), consistent with diffuse lymphangiectasia. More readily apparent on MRI were superficial inguinal lymphangiectasia (Fig. 1K) and mild scrotal subcutaneous lymphangiectasia (not shown).



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Fig. 1G 23-year-old man with filariasis. Enhanced CT scans of abdomen (G) and pelvis (H) show nonenhancing low-density material in retroperitoneum and pelvis surrounding aorta, inferior vena cava, proximal renal vessels, and iliac vessels (arrowheads). Central attenuation value of this diffusely distributed material ranged from 8 to 27 H in retroperitoneum and from 22 to 30 H along common iliac and external iliac vessels.

 


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Fig. 1H 23-year-old man with filariasis. Enhanced CT scans of abdomen (G) and pelvis (H) show nonenhancing low-density material in retroperitoneum and pelvis surrounding aorta, inferior vena cava, proximal renal vessels, and iliac vessels (arrowheads). Central attenuation value of this diffusely distributed material ranged from 8 to 27 H in retroperitoneum and from 22 to 30 H along common iliac and external iliac vessels.

 


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Fig. 1I 23-year-old man with filariasis. Single-shot fast spin-echo images (12,500/99) show high-signal-intensity confluence of dilated lymphatic ducts and vessels in retroperitoneum and pelvis.

 


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Fig. 1J 23-year-old man with filariasis. Single-shot fast spin-echo images (12,500/99) show high-signal-intensity confluence of dilated lymphatic ducts and vessels in retroperitoneum and pelvis.

 


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Fig. 1K 23-year-old man with filariasis. Single-shot fast spin-echo image (12,500/99) shows superficial inguinal lymphangiectasia (arrowheads) more readily than CT images.

 



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Fig. 1L 23-year-old man with filariasis. High-power microscopic view of microfilaria of Wuchereria bancrofti obtained from peripheral blood smear shows presence of distinct sheath and absence of nuclei in tail. (Wright-Giemsa stain)

 
On reviewing the fine-needle aspiration sample of the patient's inguinal lymph node, a single microfilaria was identified. His peripheral blood smear revealed many motile microfilariae, and a Wright-Giemsa-stained buffy coat confirmed the diagnosis of Wuchereria bancrofti (Fig. 1L).

The patient was treated with a half dose of ivermectin, followed 1 week later with diethylcarbamazine obtained from the Centers for Disease Control and Prevention. His treatment was complicated by severe testicular pain, mild fever, anorexia, nausea, headache, and mild eosinophilia. He returned to duty in good health.


Discussion
Top
Introduction
Case Report
Discussion
References
 
Human lymphatic filariasis is caused by infections with W. bancrofti, Brugia malayi, or Brugia timori. These parasites are found in many tropical and subtropical areas of the world. The adult worms live in the lymphatics throughout the body and cause extensive lymphangiectasia by obstructing lymph flow. Filariasis is the most common cause of acquired lymphedema in the world [1]. Interestingly, our patient had neither scrotal nor lower extremity edema.

Chest CT revealed a tubular structure in the posterior mediastinum, coursing along the thoracic spine. Its central attenuation value ranged from 15 H in a more distended segment to 32 H in the least distended portion, which was behind the left atrium. The low-density tubular structure in the posterior mediastinum of this patient is a distended thoracic duct. The thoracic duct collects lymph from most body tissues and transmits it back into the blood stream. The duct originates in the abdomen anterior to the second lumbar vertebra at the cisterna chyli and then ascends into the thorax through the aortic hiatus of the diaphragm slightly to the right of the midline. Within the posterior mediastinum of the thorax and still coursing just ventral to the vertebral column, the thoracic duct gradually crosses the midline to the left. The duct then ascends into the root of the neck on the left side and drains into the left subclavian vein near the junction of the left internal jugular vein [2].

An abdominal CT scan revealed low-attenuation material distributed in the retroperitoneum and pelvis that showed no enhancement with IV contrast material. The central attenuation value ranged from 8 to 27 H in the retroperitoneum and 22 to 30 H in the pelvis along the iliac vessels. No discrete mass was identified associated with this diffuse abnormality. MR images clearly revealed nonenhancing confluence of prominent lymphatic ducts and vessels. Superficial inguinal lymphangiectasia and mild scrotal subcutaneous lymphangiectasia were also more readily evident on heavily T2-weighted images.

Case et al. [3] used MRI to detect dilated lymphatic vessels in ferrets infected with B. malayi. In 1999, Blacksin et al. [4] reported the first description of MRI findings in a human, a case of bancroftian filariasis affecting the ankle joint [4]. Witte et al. [5] described the potential use of MRI, particularly fat-saturated T2-weighted images, for the evaluation of the lymphatic system. Schick et al. [6] described cystic lymph node enlargement of the neck on MRI in a patient with filariasis.

This case shows the distended thoracic duct on CT as a nonenhancing low-attenuation tubular structure in the posterior mediastinum. Its recognition is made easier by knowing the anatomic origin and course of the thoracic duct. Diffuse lymphangiectasia in the retroperitoneum and pelvis appears on CT as nonenhancing low-attenuation material along major vessels and is not associated with a discrete mass. MR images, particularly single-shot fast spin-echo images, a heavily T2-weighted pulse sequence, helped reveal the nonenhancing fluid-filled thoracic duct and prominent lymphatic ducts and vessels. To our knowledge, this case is the first reported case of distended thoracic duct and diffuse central and peripheral lymphangiectasia in a patient with active filarial infection.


References
Top
Introduction
Case Report
Discussion
References
 

  1. Szuba A, Rockson SG. Lymphedema: classification, diagnosis and therapy. Vasc Med 1998;3 : 145-156[Abstract/Free Full Text]
  2. Clemente CD. Anatomy: a regional atlas of the human body, 3rd ed. Baltimore, MD: Urban & Schwarzenberg,1987 : Figures 222, 223
  3. Case TC, Unger E, Bernas MJ, et al. Lymphatic imaging in experimental filariasis using magnetic resonance. Invest Radiol 1992; 27:293 -297[Medline]
  4. Blacksin MF, Lin SS, Trofa AF. Filariasis of the ankle: magnetic resonance imaging. Foot Ankle Int 1999;20 : 738-740[Medline]
  5. Witte CL, Witte MH, Unger EC, et al. Advances in imaging of lymph flow disorders. RadioGraphics 2000;20 : 1697-1719[Abstract/Free Full Text]
  6. Schick C, Thalhammer A, Balzer JO, et al. Cystic lymph node enlargement of the neck: filariasis as a rare differential diagnosis in MRI. Eur Radiol 2002;12 : 2349-2351[Medline]

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