Journal of the Pancreas Open Access

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Case Report - (2017) Volume 18, Issue 3

Subcutaneous and Muscular Metastasis of Pancreatic Adenocarcinoma

Kemal Murat Haberal, Fuldem Yıldırım Dönmez, Ebru Şebnem Ayva, Mehmet Çoşkun

Department of Radiology, Başkent University, Turkey

*Corresponding Author:
Kemal Murat Haberal
Department of Radiology
Başkent University, Turkey
Tel: + 03122036868
E-mail: kmhbjk@hotmail.com / kmhaberal@baskent.edu.tr

Received February 24th, 2017-Accepted April 07th, 2017

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Abstract

Soft tissue metastasis from pancreatic cancer is a very rare entity. We reported a case presenting with multiorgan and soft tissue metastasis on computed tomography. Computed tomography scan showed a hypovascular mass in the pancreatic body and tail. Computed tomography guided biopsy from muscle metastases diagnosed an undifferentiated tumor. Based on clinical, radiological and pathological correlation, the diagnosis of pancreatic adenocarcinoma was established. There are few reported cases of skeletal muscle metastasis from pancreatic cancer. Immunohistochemical staining and imaging findings should be used together to determine the correct diagnosis.

Keywords

Pancreatic Neoplasms; Pathology

INTRODUCTION

Pancreatic cancer is one of the most lethal cancers, almost all patients develop metatases [1]. The most frequent sites for metastasis are lymph nodes, lung, liver, adrenal glands and bone [2]. Skeletal muscle and subcutaneous tissue are very unusual sites of metastasis [3]. Herein, we present a pancreatic cancer with multiple muscular and subcutaneous metastases.

CASE REPORT

A Fifty-year-old man was admitted to our emergency department with jaundice and left flank pain. His past medical history was unremarkable. Sonography revealed a distended gall bladder with thickened wall and biliary sludge inside, bilateral adrenal masses, a hypoechoic mass in the midline at the pancreatic zone. Abdominal computed tomography (CT) was requested for detailed investigation. CT scan showed a hypodense lesion, measuring 105 × 47 m in size,which was located in the body and tail and infiltrating the splenic vein (Figure 1). There were bilateral adrenal masses, paraceliac, peripancreatic lymph nodes, lung nodules, bilateral muscular lesions in the gluteal muscles and subcutaneous nodules in the right buttock (Figures 1, 2). Intramuscular lesions were hypo to isodense in the precontrast scans and showed peripheral enhancement in the postcontrast series (Figure 3). No centripedal enhancement was seen in the late phase scan.

pancreas-portal-hypodense-pancreas

Figure 1. Portal phase axial CT scan shows hypodense solid lesion in the pancreas tail (red arrow) and adrenal metastases (yellow arrows).

pancreas-axial-subcutaneos-buttock

Figure 2. Axial CT scan shows a solid lesion in the subcutaneos fat tissue at the right buttock (red arrow).

pancreas-precontrast-enhancedaxial

Figure 3. (a). Precontrast and (b). contrast enhancedaxial CT scan shows peripheral enhancement of the solid lesion in the left gluteus medius muscle.

A CT guided biopsy from the intramuscular mass in the left gluteus medius was performed. Histological and immunochemistry studies showed an undifferentiated tumor inwhich most of the tumor cells were positive for cytokeratin AE1/AE3, 19, 7, 5/6 and vimentin. Neuroendocrine markers, S-100 protein, cytokeratin 20, napsin, thyroid transcription factor-1 (TTF-1), prostatic acid phosphotase (PSAP), melonama antigen (Melan A) were negative (Figure 4). According to the clinical, biological, radiological and histological findings, all the muscular metastasis was most probably originated from an undifferentianted pancreatic adenocarcinoma.

pancreas-cytokeratin-cytoplasm

Figure 4. (a, b). Cytokeratin 7, 19 positivity in the cytoplasm of tumor cells (×400, 3,3′diaminobenzidine ). Microscopic view of an undifferentiated tumor. It is composed of small round tumor cells with small round hyperchromatic pleomorphic nuclei. (c, d). The cells are arranged in nests or cords (X200, Hematoxyline&eosin). (e). Pan cytokeratin (AE1/AE3) positivity in the cytoplasm of tumor cells (×400, 3,3′diaminobenzidine). (f). Vimentin; Cytoplasmic expression of Vimentin in tumor cells (×200, 3,3′diaminobenzidine).

A few days later the patient had a sudden onset abdominal pain, CT scan at that time revealed an intestinal perforation. Unfotunately after surgical operation for the perforated intetine, patient passed away within a few days.

DISCUSSION

In autopsy series, the reported incidence of intramuscular metastasis ranges from 0.8 to 16% [4]. The most common malignancies with metastasis to the soft tissues are lung, kidney and colon carcinoma and the most common histologic type is adenocarcinoma [5]. Soft tissue metastasis from pancreatic carcinoma is extremely rare, in a series of 121 cases by Damron et al. only one case was reported [6]. Leinung et al. in a series of 98 cases and Tuoheti et al. in a series of 12 cases described soft tissue metastasis however none of the primary site of origin was pancreas [7, 8]. Mathis et al. reported that metastases to the soft tissues usually appeared with other metastases in patients with advanced dissease and the most frequent localization was the lower limbs [9]. Our case also had adrenal gland, lymph node and lung metastasis along with gluteal muscle metastasis.

In spite of the fact that skeletal muscle and subcutaneous tissue represents 50-55% of total body mass, hematogenous metastases to these areas are uncommon. Different theories have been implicated to explain this phenomenon such as lactic acid metabolism, changes in pH, variability of blood flow and tissue pressure influenced by adrenergic receptors, local temperature and presence of protease inhibitors [10].

Most intramuscular lesions are defined on CT imaging, because it is the most commonly used imaging modality in oncologic screening. They appeared as a central hypodense lesions with an enhancing rim [11]. The lesions in our case had similar imaging charasteristics.

Soft tissue metastases are frequently a sign for advanced dissease, they could be the first clinical sign. Most of the soft tissue metastases are poorly differentiated and it is hard to determine the primary origin with immunohistochemical examination. Therefore for a correct diagnosis, the radiological and clinical findings are necessary [5, 10]. We also had to use a wide panel of immunochemical examination with radiological findings to achieve a correct diagnosis in our case.

The prognosis after the diagnosis of skeletal muscle metastases is poor because of the fact that skeletal muscle metastases usuallly occur late and in the presence of disseminated dissease such as this case [6, 11].

Soft tissue metastasis from pancreatic carcinoma is very rare. Immunohisochemical staining and imaging findings should be used together to determine the correct diagnosis.

Conflict of Interest

The authors have no potential conflict of interest.

References