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[Pathology] Atlas of Mediastinal Paraganglioma

These are pictures of Mediastinal Paraganglioma. This is a part in the Atlas of Anatomic Pathology book


Mediastinal Paraganglioma  

Fig. 3.101  Paragangliomas may arise from displaced paraganglia in  the mediastinum. The tumors are distinguished grossly from neuroen- docrine carcinomas by their good circumscription and encapsulation
Fig. 3.101 Paragangliomas may arise from displaced paraganglia in the 
mediastinum. The tumors are distinguished grossly from neuroendocrine 
carcinomas by their good circumscription and encapsulation

Fig. 3.102 Cut section of a paraganglioma shows a well- circumscribed and encapsulated tumor with a homogeneous tan color and soft cut surface with foci of stromal hemorrhage
Fig. 3.102 Cut section of a paraganglioma shows a well- circumscribed
and encapsulated tumor with a homogeneous tan color and soft cut 
surface with foci of stromal hemorrhage  


Fig. 3.103 The histologic hallmark of mediastinal paraganglioma is a nested (“tzellballen”) pattern of growth. Unlike neuroendocrine carcinomas of the thymus, paragangliomas do not show trabecular, diffuse, microacinar, or ribbon-like patterns of growth
Fig. 3.103 The histologic hallmark of mediastinal paraganglioma is a
nested (“tzellballen”) pattern of growth. Unlike neuroendocrine carcinomas 
of the thymus, paragangliomas do not show trabecular, diffuse,
microacinar, or ribbon-like patterns of growth
  

Fig. 3.104 One of the distinguishing features of paraganglioma is the presence of endocrine atypia, characterized by scattered large, atypical cells with nucleomegaly in the absence of mitotic activity
Fig. 3.104 One of the distinguishing features of paraganglioma is the
presence of endocrine atypia, characterized by scattered large, atypical
cells with nucleomegaly in the absence of mitotic activity
  

Fig. 3.105 The cells in mediastinal paragangliomas are most often characterized by abundant eosinophilic cytoplasm, but in some instances, they can be composed predominantly of cells with abundant clear cytoplasm
Fig. 3.105 The cells in mediastinal paragangliomas are most often
characterized by abundant eosinophilic cytoplasm, but in some
instances, they can be composed predominantly of cells with abundant
clear cytoplasm
 
 

Fig. 3.106 Rare cases of mediastinal paraganglioma can also show prominent spindling of the tumor cells, which is most often a focal phenomenon. The diagnosis can be made by identifying the more conventional components of the lesion
Fig. 3.106 Rare cases of mediastinal paraganglioma can also show
prominent spindling of the tumor cells, which is most often a focal phenomenon. 
The diagnosis can be made by identifying the more conventional components of the lesion  

Mediastinal paragangliomas sometimes can undergo regressive changes of the stroma, including stromal sclerosis and angiectatic vessels
Fig. 3.107 Mediastinal paragangliomas sometimes can undergo
regressive changes of the stroma, including stromal sclerosis and angiectatic vessels. 
These changes can sometimes be so extensive that they
obscure the lesion, and ample sampling to identify the more conventional
 tumor component is required for the correct diagnosis  

Fig. 3.108 An unusual variant of mediastinal paraganglioma is characterized 
by extensive stromal sclerosis that sometimes can obscure the
underlying tumor
  

Most mediastinal paragangliomas are characterized by strong expression of neuroendocrine markers
Fig. 3.109 Most mediastinal paragangliomas are characterized by
strong expression of neuroendocrine markers. This image shows cytoplasmic 
positivity for chromogranin in a mediastinal paraganglioma.
Unlike primary neuroendocrine carcinomas of the thymus, however,
these tumors are negative for cytokeratin
  
Suggested Reading

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Crona J, Bjorklund P, Welin S, Kozlovacki G, Oberg K, Granberg D. Treatment, prognostic markers and survival in thymic neuroendocrine tumors. A study from a single tertiary referral centre. Lung Cancer. 2013;79:289–93.

Economopoulus GC, Lewis Jr JW, Lee MW, Silverman NA. Carcinoid tumors of the thymus. Ann Thorac Surg. 1990;50:58–61. 

Floros D, Dosios T, Tsourdis A, Yiatromanolakis N. Carcinoid tumor of the thymus with multiple endocrine adenomatosis. Pathol Res Pract. 1982;175:404–9.

Gal AA, Kornstein MJ, Cohen C, Duarte IG, Miller JI, Mansour KA. Neuroendocrine tumors of the thymus: a clinicopathological and prognostic study. Ann Thorac Surg. 2001;72:1179–82.

Klemm KM, Moran CA, Suster S. Pigmented thymic carcinoids. A clinicopathological and immunohistochemical study of 2 cases. Mod Pathol. 1999;12:946–8.

Montpreville VT, Machiarini P, Dulmet E. Thymic neuroendocrine carcinoma (carcinoid): a clinicopathologic study of 14 cases. J Thorac Cardiovasc Surg. 1996;111:134–41.

Moran CA, Suster S. Angiomatous neuroendocrine carcinoma of the thymus: report of a distinctive morphological variant of neuroendocrine tumor of the thymus resembling a vascular neoplasm. Hum
Pathol. 1999a;30:635–9.

Moran CA, Suster S. Spindle cell neuroendocrine carcinomas of the thymus (spindle cell thymic carcinoid): a clinicopathologic and immunohistochemical study of seven cases. Mod Pathol. 1999b;12:587–91.

Moran CA, Suster S. Neuroendocrine carcinoma (carcinoid) of the thymus: A clinicopathologic analysis of 80 cases. Am J Clin Pathol. 2000a;114:100–10.

Moran CA, Suster S. Primary neuroendocrine carcinoma (carcinoid) of the thymus with prominent oncocytic features: clinicopathologic study of 22 cases. Mod Pathol. 2000b;13:489–94. 

Moran CA, Suster S. Thymic neuroendocrine carcinomas with combined features ranging from well-differentiated (carcinoid) to small cell carcinoma: a clinicopathologic and immunohistochemical study of 11 cases. Am J Clin Pathol. 2000c;113:345–50.

Moran CA, Suster S. Cystic well-differentiated neuroendocrine carcinoma (carcinoid tumor). A clinicopathologic and immunohistochemical study of two cases. Am J Clin Pathol. 2006a;126:377–80. 

Moran CA, Suster S. Spectrum of pathologic features in neuroendocrine neoplasms of the mediastinum. Pathol Case Rev. 2006b;11:199–205.

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Suster S, Moran CA. Thymic carcinoid with prominent mucinous stroma: report of a distinctive morphologic variant of thymic neuroendocrine neoplasm. Am J Surg Pathol. 1995;19:1277–85.

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Wick MR, Carney JA, Bernatz PE, Brown LR. Primary mediastinal carcinoid tumors. Am J Surg Pathol. 1982;6:195–205.

Wick MR, Scheithauer BW. Oat cell carcinoma of the thymus. Cancer. 1982;49:1652–7.

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Free Medical Atlas: [Pathology] Atlas of Mediastinal Paraganglioma
[Pathology] Atlas of Mediastinal Paraganglioma
These are pictures of Mediastinal Paraganglioma. This is a part in the Atlas of Anatomic Pathology book
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